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Disease Term | Allelic Composition | Genetic Background | Reference | Phenotypes | ||||
![]() ![]() | achondrogenesis type II | Col2a1tm1Prc/Col2a1tm1Prc | involves: 129 | J:117910 | View | |||
adult-onset autosomal dominant demyelinating leukodystrophy | Tg(Lmnb1)1Yfu/0 | involves: C57BL/6J | J:197168 | View | ||||
advanced sleep phase syndrome 1 | Per2M1Btlr/Per2M1Btlr | C57BL/6J-Per2M1Btlr | J:264638 | View | ||||
age related macular degeneration 4 | Cfhtm1Mbo/Cfhtm1Mbo | B6.129-Cfhtm1Mbo | J:203471 | View | ||||
age related macular degeneration 12 | Cx3cr1tm1Zm/Cx3cr1tm1Zm | C.129-Cx3cr1tm1Zm | J:127548 | View | ||||
age related macular degeneration 12 | Cx3cr1tm1Zm/Cx3cr1tm1Zm | involves: 129 * C57BL/6 | J:127548 | View | ||||
Alexander disease | Gfaptm2Mes/Gfap+ | involves: 129S6/SvEvTac * 129S7/SvEvBrd * FVB/N | J:114689 | View | ||||
Alexander disease |
Gfaptm2Mes/Gfap+ Tg(GFAP)10Mes/0 |
involves: 129S6/SvEvTac * 129S7/SvEvBrd * FVB/N | J:114689 | View | ||||
Alexander disease |
Gfaptm2Mes/Gfap+ Tg(GFAP)10Mes/0 |
involves: 129S7/SvEvBrd * FVB/N | J:146191 | View | ||||
Alexander disease | Gfaptm3Mes/Gfap+ | involves: 129S6/SvEvTac * 129S7/SvEvBrd * FVB/N | J:114689 | View | ||||
Alzheimer's disease 3 |
Psen1tm1Lpr/Psen1tm1Lpr Tg(Thy1-APPSL)28Lpr/0 |
either: 129/Sv or (involves: 129/Sv * C57BL/6) | J:93770 | View | ||||
Alzheimer's disease 3 | Psen1tm1Mpm/Psen1tm1Mpm | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:51950 | View | ||||
Alzheimer's disease 3 | Psen1tm1Mpm/Psen1tm1Pcw | involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6 | J:91277 | View | ||||
Alzheimer's disease 3 | Psen1tm1Shn/Psen1tm1Shn | involves: 129S7/SvEvBrd * C57BL/6 | J:40365 | View | ||||
Alzheimer's disease 3 | Psen1tm1Tak/Psen1+ | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:108326 | View | ||||
Alzheimer's disease 3 |
Psen1tm1Vln/Psen1tm1Vln Tg(Thy1-cre)1Vln/0 |
involves: FVB/N | J:87229 | View | ||||
amelogenesis imperfecta type 1B | EnamRgsc395/Enam+ | involves: C57BL/6JJcl * DBA/2J | J:96349 | View | ||||
amelogenesis imperfecta type 1B | EnamRgsc514/Enam+ | involves: C57BL/6JJcl * DBA/2J | J:96349 | View | ||||
amelogenesis imperfecta type 1B | EnamRgsc521/Enam+ | involves: C57BL/6JJcl * DBA/2J | J:96349 | View | ||||
amelogenesis imperfecta type 1B | EnamRgsc521/EnamRgsc521 | involves: C57BL/6JJcl * DBA/2J | J:96349 | View | ||||
amelogenesis imperfecta type 1B | Enamtm1.1Jcch/Enam+ | involves: C57BL/6 | J:223123 | View | ||||
amelogenesis imperfecta type 1B | Enamtm1.1Jcch/Enamtm1.1Jcch | involves: C57BL/6 | J:223123 | View | ||||
amyotrophic lateral sclerosis type 1 | Sod1m1H/Sod1m1H | involves: C3H/HeH * C57BL/6J | J:219360 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(Sod1*G86R)M1Jwg/0 | involves: FVB/N | J:22628, J:58733, J:91800 | View | ||||
ankyloblepharon-ectodermal defects-cleft lip/palate syndrome | Trp63tm1Cmis/Trp63+ | involves: 129P2/OlaHsd * C57BL/6 | J:191121 | View | ||||
ankyrin-B-related cardiac arrhythmia | Ank2em1Melr/Ank2em1Melr | B6.Cg-Ank2em1Melr | J:338515 | View | ||||
antithrombin III deficiency | Serpinc1tm1Dwr/Serpinc1tm1Dwr | involves: 129S1/Sv * 129X1/SvJ | J:115658 | View | ||||
arrhythmogenic right ventricular dysplasia 8 |
Dsptm1Efu/Dsptm1Efu Myl2tm1(cre)Krc/Myl2+ |
involves: 129 * 129S4/SvJae * C57BL/6 | J:205990 | View | ||||
arrhythmogenic right ventricular dysplasia 10 | Dsg2tm1d(EUCOMM)Wtsi/Dsg2tm1d(EUCOMM)Wtsi | involves: C57BL/6J * C57BL/6N | J:235770 | View | ||||
arrhythmogenic right ventricular dysplasia 12 |
Juptm1.1Glr/Juptm1.1Glr A1cfTg(Myh6-cre/Esr1*)1Jmk/A1cf+ |
involves: 129S6/SvEvTac * C57BL/6 * FVB/N * SJL | J:170618 | View | ||||
arrhythmogenic right ventricular dysplasia 12 |
Juptm1.1Shou/Juptm1.1Shou Tg(Myh6-cre)2182Mds/0 |
involves: 129 * C57BL/6J | J:177567 | View | ||||
arrhythmogenic right ventricular dysplasia 12 |
Juptm1Ruiz/Jup+ Tg(Myh6-Jup*)1Ajm/0 |
involves: 129P2/OlaHsd * C57BL/6 * FVB/N | J:192719 | View | ||||
arrhythmogenic right ventricular dysplasia 12 | Tg(Myh6-Jup*)1Ajm/0 | involves: FVB/N | J:192719 | View | ||||
atrial heart septal defect 2 | Gata4tm1Grg/Gata4+ | involves: 129 * C57BL/6 | J:185124 | View | ||||
atrial heart septal defect 7 | Nkx2-5tm2.1Mwc/Nkx2-5+ | B6J.Cg-Nkx2-5tm2.1Mwc/Mwc | J:239808 | View | ||||
atrial heart septal defect 7 | Nkx2-5tm3.1Mwc/Nkx2-5+ | B6J.Cg-Nkx2-5tm3.1Mwc/Mwc | J:239808 | View | ||||
autoimmune interstitial lung, joint, and kidney disease | Copatm1.1Shum/Copa+ | B6(CBA)-Copatm1.1Shum | J:288425 | View | ||||
autosomal dominant auditory neuropathy 1 | Tg(CAG-Diap3)924Lesp/0 | FVB/NJ-Tg(CAG-Diap3)924Lesp | J:193237 | View | ||||
autosomal dominant auditory neuropathy 1 | Tg(CAG-Diaph3)771Lesp/0 | FVB/NJ-Tg(CAG-Diaph3)771Lesp | J:193237 | View | ||||
autosomal dominant congenital deafness with onychodystrophy | Atp6v1b2tm1Yoyu/Atp6v1b2+ | involves: C57BL/6 | J:278514 | View | ||||
autosomal dominant congenital deafness with onychodystrophy | Atp6v1b2tm1Yoyu/Atp6v1b2tm1Yoyu | involves: C57BL/6 | J:278514 | View | ||||
autosomal dominant distal hereditary motor neuronopathy 2 | Hspb8tm1Vti/Hspb8tm1Vti | involves: 129S6/SvEvTac * C57BL/6J * C57BL/6NCrl | J:284796 | View | ||||
autosomal dominant hypocalcemia 1 | CasrNuf/Casr+ | either: (involves: 102/El * 102/H * C3H/He) or (involves: 102/El * C3H/He * C3H/HeH) | J:92612 | View | ||||
autosomal dominant hypocalcemia 1 | CasrNuf/CasrNuf | involves: 102/El * C3H/He | J:92612 | View | ||||
autosomal dominant hypocalcemia 2 | Gna11em1Mman/Gna11+ | C57BL/6NCrl-Gna11em1Mman | J:280180 | View | ||||
autosomal dominant hypocalcemia 2 | Gna11em1Mman/Gna11em1Mman | C57BL/6NCrl-Gna11em1Mman | J:280180 | View | ||||
autosomal dominant hypophosphatemic rickets | Fgf23tm1.1Kew/Fgf23tm1.1Kew | B6.129-Fgf23tm1.1Kew | J:180061 | View | ||||
autosomal dominant hypophosphatemic rickets |
Fgf23tm1Blan/Fgf23tm1Blan PhexHyp/Y |
Not Specified | J:94041 | View | ||||
autosomal dominant intellectual developmental disorder 7 | Dyrk1aem1Kzy/Dyrk1a+ | C57BL/6J-Dyrk1aem1Kzy | J:259596 | View | ||||
autosomal dominant intellectual developmental disorder 26 | Auts2tm1Mhos/Auts2+ | C57BL/6N-Auts2tm1Mhos | J:261355 | View | ||||
autosomal dominant intellectual developmental disorder 38 | Eef1a2em#Abb/Eef1a2+ | C57BL/6JCrl-Eef1a2em#Abb | J:296080 | View | ||||
autosomal dominant intellectual developmental disorder 39 | Myt1lem1Jdd/Myt1l+ | C57BL/6-Myt1lem1Jdd/J | J:321206 | View | ||||
autosomal dominant intellectual developmental disorder 39 | Myt1lem1Mwer/Myt1l+ | involves: C57BL/6N | J:326588 | View | ||||
autosomal dominant keratitis-ichthyosis-deafness syndrome |
Gjb2tm2.2Kwi/Gjb2+ Tg(Pgk1-cre)1Lni/0 |
involves: 129/Sv * 129P2/OlaHsd * BALB/c * C57BL/6 | J:166732 | View | ||||
autosomal dominant nocturnal frontal lobe epilepsy 3 | Chrnb2tm1.1Cont/Chrnb2tm1.1Cont | B6.129-Chrnb2tm1.1Cont | J:228269 | View | ||||
autosomal dominant nocturnal frontal lobe epilepsy 3 |
Tg(Prnp-tTA)F959Sbp/0 Tg(tetO-Chrnb2*V287L)H3Gica/0 |
involves: 129S7/SvEvBrd * FVB | J:145855 | View | ||||
autosomal dominant nonsyndromic deafness 9 | Cochtm1Mrtn/Cochtm1Mrtn | CBACa.129S4-Cochtm1Mrtn | J:140594, J:167669 | View | ||||
autosomal dominant nonsyndromic deafness 12 | Tectatm2Gpr/Tecta+ | involves: 129S/SvEv * C57BL/6J | J:101691 | View | ||||
autosomal dominant nonsyndromic deafness 12 | Tectatm3.1Gpr/Tecta+ | involves: 129S/SvEv | J:203482 | View | ||||
autosomal dominant nonsyndromic deafness 12 | Tectatm4.1Gpr/Tecta+ | involves: 129S/SvEv | J:203482 | View | ||||
autosomal dominant nonsyndromic deafness 12 | Tectatm5.1Gpr/Tecta+ | involves: 129S/SvEv | J:203482 | View | ||||
autosomal dominant nonsyndromic deafness 13 | Col11a2tm1Mne/Col11a2tm1Mne | FVB.129-Col11a2tm1Mne | J:71948 | View | ||||
autosomal dominant nonsyndromic deafness 22 | Myo6em1Bcgen/Myo6+ | involves: C57BL/6J * CBA/CaJ | J:288210 | View | ||||
autosomal dominant nonsyndromic deafness 22 | Myo6sv/Myo6sv | involves: B10.HA/(33NX)Sn * C57BL/6J | J:29898 | View | ||||
autosomal dominant nonsyndromic deafness 25 | Slc17a8tm1Selm/Slc17a8tm1Selm | involves: 129/Sv * C57BL/6 | J:139493 | View | ||||
autosomal dominant nonsyndromic deafness 36 | Tmc1dn/Tmc1dn | involves: STOCK Grhl3ct * M. m. molossinus | J:22445 | View | ||||
autosomal dominant nonsyndromic deafness 36 | Tmc1dn/Tmc1dn | STOCK Grhl3ct/J | J:236 | View | ||||
autosomal dominant nonsyndromic deafness 36 | Tmc1Mhdabth/Tmc1+ | C3HeB/FeJ-Tmc1Mhdabth/Ieg | J:86685 | View | ||||
autosomal dominant nonsyndromic deafness 41 | P2rx2em1Xzl/P2rx2+ | CBA/J-P2rx2em1Xzl | J:315007 | View | ||||
autosomal dominant nonsyndromic deafness 67 | Osbpl2em1Cya/Osbpl2em1Cya | C57BL/6-Osbpl2em1Cya | J:324115 | View | ||||
autosomal dominant osteopetrosis 2 | Clcn7tm1.1Aros/Clcn7tm1.1Aros | involves: 129P2/OlaHsd * C57BL/6N | J:273179 | View | ||||
autosomal dominant osteopetrosis 2 | Clcn7tm1.1Mawa/Clcn7+ | involves: C57BL/6J * C57BL/6N * CD-1 | J:254787 | View | ||||
autosomal dominant osteopetrosis 2 | Clcn7tm1.1Mjec/Clcn7+ | involves: 129 * 129S/SvEv * C57BL/6 | J:203761 | View | ||||
autosomal dominant osteopetrosis 2 | Clcn7tm1.1Mjec/Clcn7+ | involves: 129S/SvEv * C57BL/6 * DBA/2J | J:203761 | View | ||||
autosomal dominant osteopetrosis 2 | Clcn7tm1.1Teti/Clcn7+ | involves: 129S2/SvPas * C57BL/6 | J:203761 | View | ||||
autosomal dominant osteopetrosis 2 | Clcn7tm1.1Teti/Clcn7tm1.1Teti | involves: 129S2/SvPas * C57BL/6 | J:203761 | View | ||||
autosomal dominant osteopetrosis 2 | Clcn7tm1.1Teti/Clcn7tm1.1Teti | involves: 129S2/SvPas * CD-1 | J:203761 | View | ||||
autosomal dominant polycystic kidney disease |
Pkd2tm1.1Gwu/Pkd2tm1.1Gwu Tg(Vil1-cre)997Gum/0 |
involves: C57BL/6 * C57BL/6J * SJL | J:265516 | View | ||||
autosomal dominant pseudohypoaldosteronism type 1 | Nr3c2tm1Gsc/Nr3c2tm1Gsc | involves: 129P2/OlaHsd * C57BL/6 | J:77285 | View | ||||
Axenfeld-Rieger syndrome type 1 | Pitx2tm1Jfm/Pitx2tm1Jfm | involves: 129S4/SvJaeSor | J:57674, J:87220 | View | ||||
Axenfeld-Rieger syndrome type 1 | Pitx2tm1Jfm/Pitx2tm2Jfm | involves: 129S4/SvJaeSor | J:87220 | View | ||||
Axenfeld-Rieger syndrome type 1 | Pitx2tm1Kki/Pitx2tm1Kki | involves: 129P2/OlaHsd * C57BL | J:55455 | View | ||||
Axenfeld-Rieger syndrome type 1 | Pitx2tm1Rsd/Pitx2tm1Rsd | involves: 129S1/Sv * 129X1/SvJ | J:57673 | View | ||||
Axenfeld-Rieger syndrome type 1 | Pitx2tm1Sac/Pitx2+ | involves: 129S1/Sv * 129X1/SvJ * C57BL/6J | J:51160 | View | ||||
Axenfeld-Rieger syndrome type 1 | Pitx2tm2Sac/Pitx2+ | involves: 129S1/Sv * 129X1/SvJ * C57BL/6J | J:51160 | View | ||||
Bannayan-Riley-Ruvalcaba syndrome | Ptentm1Mak/Pten+ | involves: 129P2/OlaHsd * C57BL/6J | J:63478 | View | ||||
Bannayan-Riley-Ruvalcaba syndrome | Ptentm1Ppp/Pten+ | involves: 129S1/Sv * C57BL/6J | J:49532 | View | ||||
Bannayan-Riley-Ruvalcaba syndrome | Ptentm1Rps/Pten+ | involves: 129S1/Sv * C57BL/6J | J:53065 | View | ||||
Beare-Stevenson cutis gyrata syndrome | Fgfr2tm3Ewj/Fgfr2+ | B6.129-Fgfr2tm3Ewj | J:190491 | View | ||||
Birt-Hogg-Dube syndrome |
Flcntm1Baba/Flcntm1.1Lss Tg(Cdh16-cre)91Igr/0 |
involves: C57BL/6 * FVB/N * ICR * SJL | J:130978 | View | ||||
Birt-Hogg-Dube syndrome |
Flcntm1Btt/Flcntm1Btt Tg(Cdh16-cre)91Igr/0 |
involves: 129S4/SvJaeSor * C57BL/6 * ICR | J:143922 | View | ||||
Bosch-Boonstra-Schaaf optic atrophy syndrome | Nr2f1tm1Mjts/Nr2f1+ | involves: 129S7/SvEvBrd | J:286647 | View | ||||
brachydactyly type A1 | Ihhtm1.1Dcha/Ihhtm1.1Dcha | either: (involves: 129S/SvEv * FVB/N) or (involves: 129S/SvEv * FVB/N * ICR) | J:147878 | View | ||||
brachydactyly type A1C | Gdf5Bp-5J/Gdf5+ | C57BL/6J-Gdf5Bp-5J/GrsrJ | J:200816 | View | ||||
brachydactyly type A2 | Gdf5Bp-5J/Gdf5+ | C57BL/6J-Gdf5Bp-5J/GrsrJ | J:200816 | View | ||||
brachydactyly type C | Gdf5Bp-5J/Gdf5+ | C57BL/6J-Gdf5Bp-5J/GrsrJ | J:200816 | View | ||||
brain small vessel disease 1 | Col4a1deltaex40/Col4a1+ | B6.129S-Col4a1deltaex40 | J:215446 | View | ||||
branchiootorenal syndrome | Eya1bor/Eya1bor | C3HeB/FeJ-Eya1bor | J:54408 | View | ||||
branchiootorenal syndrome | Eya1tm1Rilm/Eya1+ | either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * BALB/c) | J:57313 | View | ||||
branchiootorenal syndrome | Eya1tm1Rilm/Eya1+ | involves: 129S1/Sv * 129X1/SvJ * C57BL/6J | J:57313 | View | ||||
branchiootorenal syndrome | Eya1tm1Rilm/Eya1tm1Rilm | either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * BALB/c) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) | J:57313 | View | ||||
branchiootorenal syndrome | Six1Cwe/Six1Cwe | C3HeB/FeJ-Six1Cwe | J:149467 | View | ||||
Brugada syndrome 1 | Scn5atm1Agrc/Scn5a+ | involves: 129 | J:166438 | View | ||||
Brugada syndrome 1 | Scn5atm1Care/Scn5a+ | FVB.129P2-Scn5atm1Care/Care | J:128657 | View | ||||
Brugada syndrome 7 | Scn3btm1Clhh/Scn3btm1Clhh | 129S/SvEv-Scn3btm1Clhh | J:177262 | View | ||||
bullous congenital ichthyosiform erythroderma | Krt2Mhdadsk2/Krt2+ | C3HeB/FeJ-Krt2Mhdadsk2/Ieg | J:81301 | View | ||||
bullous congenital ichthyosiform erythroderma | Krt2Mhdadsk2/Krt2Mhdadsk2 | involves: C3HeB/FeJ * C57BL/6J | J:81301 | View | ||||
CADASIL 1 |
Gt(ROSA)26Sortm2(NOTCH3*C455R)Sat/Gt(ROSA)26Sor+ Notch3Gt(PST033)Byg/Notch3Gt(PST033)Byg Tg(Tagln-cre)1Her/0 |
involves: 129 * C57BL/6 * SJL | J:171887 | View | ||||
CADASIL 1 |
Gt(ROSA)26Sortm3(NOTCH3*R1031C)Sat/Gt(ROSA)26Sor+ Notch3Gt(PST033)Byg/Notch3Gt(PST033)Byg Tg(Tagln-cre)1Her/0 |
involves: 129 * C57BL/6 * SJL | J:171887 | View | ||||
CADASIL 1 |
Notch1tm1Grid/Notch1+ Notch3tm1Grid/Notch3tm1Grid |
involves: 129S1/Sv * C57BL/6 | J:227333 | View | ||||
CADASIL 1 | Notch3hpbk/Notch3hpbk | C57BL/6J-Notch3hpbk/GrsrJ | J:222308 | View | ||||
CADASIL 1 | Notch3tm1.1Dwr/Notch3+ | involves: 129S/SvEv * Swiss | J:191454 | View | ||||
CADASIL 1 | Notch3tm1.1Dwr/Notch3tm1.1Dwr | involves: 129S/SvEv * Swiss | J:191454 | View | ||||
campomelic dysplasia | Sox9Bbfc/Sox9+ | C57BL/6J-Sox9Bbfc/GrsrJ | J:223062 | View | ||||
campomelic dysplasia | Sox9tm1.1Gsr/Sox9+ | involves: 129P2/OlaHsd * C57BL/6 | J:75124 | View | ||||
campomelic dysplasia | Sox9tm1.2Ksec/Sox9+ | involves: 129S/SvEv * C57BL/6 * FVB/N | J:332093 | View | ||||
campomelic dysplasia | Sox9tm1Crm/Sox9+ | involves: 129S7/SvEvBrd * C57BL/6 * CD-1 | J:69875 | View | ||||
campomelic dysplasia |
Sox9tm1Gsr/Sox9+ Tg(Pdx1-cre)6Cvw/0 |
involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J * CBA * FVB/N | J:141017 | View | ||||
campomelic dysplasia |
Sox9tm2Crm/Sox9+ Tg(Col2a1-cre)1Bhr/0 |
involves: 129S7/SvEvBrd * C57BL/6 * SJL | J:79879 | View | ||||
campomelic dysplasia |
Sox9tm2Crm/Sox9+ Tg(Prrx1-cre)1Cjt/0 |
involves: 129S7/SvEvBrd * C57BL/6J * SJL/J | J:79879 | View | ||||
campomelic dysplasia |
Sox9tm2Crm/Sox9tm2Crm Tg(Col2a1-cre)1Bhr/0 |
involves: 129S7/SvEvBrd * C57BL/6 * SJL | J:79879 | View | ||||
campomelic dysplasia |
Sox9tm2Crm/Sox9tm2Crm Tg(Prrx1-cre)1Cjt/0 |
involves: 129S7/SvEvBrd * C57BL/6J * SJL/J | J:79879 | View | ||||
Carney complex | Prkar1atm1.1Lsk/Prkar1a+ | involves: 129S1/Sv * 129X1/SvJ | J:98799 | View | ||||
Carney complex | Prkar1atm1.1Lsk/Prkar1a+ | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:160299 | View | ||||
Carney complex |
Prkar1atm1.2Lsk/Prkar1atm1.2Lsk Tg(Tyr-cre)3Gfk/0 |
either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) | J:98799 | View | ||||
Carney complex | Prkar1atm1Gsm/Prkar1a+ | involves: 129X1/SvJ | J:93393 | View | ||||
cataract 1 multiple types | Gja8No2/Gja8+ | involves: 101 * C3H | J:49492 | View | ||||
cataract 1 multiple types | Gja8No2/Gja8No2 | involves: 101 * C3H | J:49492 | View | ||||
cataract 1 multiple types | Gja8R205G/Gja8R205G | B6.Cg-Gja8R205G | J:195727 | View | ||||
cataract 1 multiple types | Gja8tm1Paul/Gja8tm1Paul | involves: 129S4/SvJae * C57BL/6J | J:50894 | View | ||||
cataract 2 multiple types | CrygcChl3/Crygc+ | involves: 102/El * C3H/El | J:73804 | View | ||||
cataract 2 multiple types | CrygcChl3/CrygcChl3 | involves: 102/El * C3H/El | J:73804 | View | ||||
cataract 3 multiple types | Crybb2Aey2/Crybb2+ | C3HeB/FeJ-Crybb2Aey2 | J:70508 | View | ||||
cataract 3 multiple types | Crybb2Lop19/Crybb2+ | SJL/J-Crybb2Lop19/BocJ | J:187061 | View | ||||
cataract 3 multiple types | Crybb2Phil/Crybb2Phil | Swiss Webster | J:11126 | View | ||||
cataract 4 multiple types | CrygdAey4/Crygd+ | C3HeB/FeJ-CrygdAey4 | J:78154 | View | ||||
cataract 4 multiple types | CrygdAey4/CrygdAey4 | C3HeB/FeJ-CrygdAey4 | J:78154 | View | ||||
cataract 5 multiple types | Hsf4ldis1/Hsf4ldis1 | involves: C57BL/6 * CAST/EiJ * RIIIS/J | J:179658 | View | ||||
cataract 5 multiple types | Tg(Hsf4/EGFP)N7Spbh/0 | C57BL/6-Tg(Hsf4/EGFP)N7Spbh | J:230205 | View | ||||
cataract 6 multiple types | Epha2Gt(KST085)Byg/Epha2Gt(KST085)Byg | involves: 129P2/OlaHsd * C57BL/6 * FVB/N | J:151310 | View | ||||
cataract 9 multiple types | CryaaAey7/Cryaa+ | C3HeB/FeJ-CryaaAey7/Ieg | J:72928 | View | ||||
cataract 9 multiple types | CryaaAey7/CryaaAey7 | C3HeB/FeJ-CryaaAey7/Ieg | J:72928 | View | ||||
cataract 9 multiple types | Cryaalop18/Cryaalop18 | involves: CBA/CaGnLeJ | J:34933 | View | ||||
cataract 9 multiple types | Cryaatm1.1Ady/Cryaa+ | involves: 129 * C57BL/6 | J:132296 | View | ||||
cataract 9 multiple types | Cryaatm1.1Ady/Cryaatm1.1Ady | involves: 129 * C57BL/6 | J:132296 | View | ||||
cataract 9 multiple types | Cryaatm1Ady/Cryaa+ | involves: 129 | J:157274 | View | ||||
cataract 9 multiple types | Cryaatm1Ady/Cryaatm1Ady | involves: 129 | J:157274 | View | ||||
cataract 9 multiple types | Cryaatm1Wawr/Cryaatm1Wawr | involves: 129/Sv * 129S4/SvJae | J:38210 | View | ||||
cataract 9 multiple types | Cryaatm1Wawr/Cryaatm1Wawr | involves: 129S4/SvJae * C57BL/6 * DBA/2 | J:38210 | View | ||||
cataract 10 multiple types | Cryba1Po1/Cryba1+ | C3HeB/FeJ-Cryba1Po1 | J:58912 | View | ||||
cataract 10 multiple types | Cryba1Po1/Cryba1Po1 | C3HeB/FeJ-Cryba1Po1 | J:58912 | View | ||||
cataract 14 multiple types | Gja3tm1.1Vmb/Gja3+ | involves: 129 * C57BL/6 | J:227244 | View | ||||
cataract 14 multiple types | Gja3tm1.1Vmb/Gja3tm1.1Vmb | involves: 129 * C57BL/6 | J:227244 | View | ||||
cataract 15 multiple types | MipCat-Fr/MipCat-Fr | involves: A/J | J:31574 | View | ||||
cataract 15 multiple types | MipCat-Lop/Mip+ | involves: STOCK Rb(6.15)1Ald | J:31574 | View | ||||
cataract 15 multiple types | MipCat-Tohm/MipCat-Tohm | involves: DDI | J:82971 | View | ||||
cataract 15 multiple types | MipCts/Mip+ | involves: C57BL/6J * CTS/Shi | J:196356 | View | ||||
cataract 15 multiple types | MipCts/MipCts | CTS/Shi | J:196356 | View | ||||
cataract 15 multiple types | MipHfi/Mip+ | involves: 101 * C3H | J:14285 | View | ||||
cataract 15 multiple types | MipHfi/MipHfi | involves: 101 * C3H | J:14285 | View | ||||
cataract 16 multiple types | Cryabtm1.1Ady/Cryabtm1.1Ady | involves: 129X1/SvJ * C57BL/6 | J:210399 | View | ||||
cataract 20 multiple types | CrygsOpj/Crygs+ | involves: 102 * C3H/He * T STOCK | J:34877, J:68109 | View | ||||
cataract 20 multiple types | CrygsOpj/CrygsOpj | involves: 102 * C3H/He * T STOCK | J:34877, J:68109 | View | ||||
cataract 20 multiple types | Crygsrncat/Crygsrncat | Kunming | J:77271 | View | ||||
cataract 21 multiple types | MafOfl/Maf+ | either: 102/ElH or C3H/HeH | J:82475 | View | ||||
cataract 30 | Tg(Vim*R113C)1Tmm/0 | B6.CBA-Tg(Vim*R113C)1Tmm | J:145782 | View | ||||
cataract 39 multiple types | CrygbClapper/Crygb+ | C57BL/6J-CrygbClapper | J:100851 | View | ||||
cataract 39 multiple types | CrygbClapper/CrygbClapper | C57BL/6J-CrygbClapper | J:100851 | View | ||||
cataract 39 multiple types | CrygbNop/Crygb+ | Not Specified | J:7589 | View | ||||
cataract 39 multiple types | CrygbNop/CrygbNop | Not Specified | J:7589 | View | ||||
cataract 39 multiple types | CrygbS11R/Crygb+ | A/J-CrygbS11R | J:132502 | View | ||||
cataract 39 multiple types | CrygbS11R/CrygbS11R | A/J-CrygbS11R | J:132502 | View | ||||
central precocious puberty 2 | Mkrn3em1Rhu/Mkrn3+ | involves: C57BL/6 | J:305000 | View | ||||
cerebellar ataxia type 42 | Cacna1gem1Ftan/Cacna1g+ | C57BL/6NCrSlc-Cacna1gem1Ftan | J:278129 | View | ||||
cerebellar ataxia type 42 | Cacna1gem1Ftan/Cacna1gem1Ftan | C57BL/6NCrSlc-Cacna1gem1Ftan | J:278129 | View | ||||
cerebrocostomandibular syndrome |
E2f1Tg(Wnt1-cre)2Sor/E2f1+ Snrpbem1Lajm/Snrpb+ |
involves: C3H * C57BL/6 * C57BL/6J * CD1 | J:326544 | View | ||||
Charcot-Marie-Tooth disease axonal type 2K | Gdap1tm1.2Geno/Gdap1tm1.2Geno | involves: 129 * C57BL/6 | J:224701 | View | ||||
Charcot-Marie-Tooth disease axonal type 2O | Dync1h1tm1.1Sjki/Dync1h1+ | involves: 129 * 129S1/SvImJ * C57BL/6 * C57BL/6J | J:264493 | View | ||||
Charcot-Marie-Tooth disease axonal type 2P | Lrsam1Gt(RRK461)Byg/Lrsam1Gt(RRK461)Byg | involves: 129P2/OlaHsd | J:196447 | View | ||||
Charcot-Marie-Tooth disease axonal type 2Q | Dhtkd1tm1Mmgu/Dhtkd1tm1Mmgu | involves: 129S6/SvEvTac * C57BL/6J | J:288186 | View | ||||
Charcot-Marie-Tooth disease axonal type 2Q | Dhtkd1tm1Zgwg/Dhtkd1tm1Zgwg | involves: C57BL/6 | J:267178 | View | ||||
Charcot-Marie-Tooth disease axonal type 2Z | Morc2aem1Snupy/Morc2a+ | involves: C57BL/6 | J:341847 | View | ||||
Charcot-Marie-Tooth disease dominant intermediate C | Yars1tm1.1Rwb/Yars1tm1.1Rwb | involves: C57BL/6N * FVB/N | J:310162 | View | ||||
Charcot-Marie-Tooth disease type 1A | Pmp22Tr-2J/Pmp22+ | C57BL/6J-Pmp22Tr-2J/GrsrJ | J:201866 | View | ||||
Charcot-Marie-Tooth disease type 1A | Pmp22Tr-J/Pmp22+ | B6.Cg-Pmp22Tr-J Krt25Re/+ +/J | J:3394, J:101812 | View | ||||
Charcot-Marie-Tooth disease type 1A | Pmp22Tr-J/Pmp22+ | involves: C57BL/6 | J:3394, J:98231 | View | ||||
Charcot-Marie-Tooth disease type 1A | Tg(Pmp22)247Ueli/0 | involves: C3H * C57BL/6 | J:98118 | View | ||||
Charcot-Marie-Tooth disease type 1A | Tg(Pmp22)My41Clh/0 | involves: C57BL/6J * CBA/Ca | J:76795 | View | ||||
Charcot-Marie-Tooth disease type 1A |
Tg(PMP22-tTA)JY13Clh/0 Tg(tetO/CMV-Pmp22)JP18Clh/0 |
involves: C57BL/6J * CBA/Ca | J:69545 | View | ||||
Charcot-Marie-Tooth disease type 1B | Mpztm1Msch/Mpz+ | involves: 129S7/SvEvBrd | J:42838 | View | ||||
Charcot-Marie-Tooth disease type 1B |
Mpztm1Msch/Mpz+ Tg(Mpz*S63X)31Mes/0 |
involves: 129S7/SvEvBrd * FVB/N | J:105751 | View | ||||
Charcot-Marie-Tooth disease type 1B | Mpztm1Msch/Mpztm1Msch | involves: 129S7/SvEvBrd | J:42838 | View | ||||
Charcot-Marie-Tooth disease type 1B | Mpztm3.1Wra/Mpz+ | FVB.129S2(Cg)-Mpztm3.1Wra | J:241742 | View | ||||
Charcot-Marie-Tooth disease type 1B | Mpztm3.1Wra/Mpztm3.1Wra | FVB.129S2(Cg)-Mpztm1.1Wra | J:241742 | View | ||||
Charcot-Marie-Tooth disease type 1B | Tg(Mpz)88.1Mfel/0 | FVB/N-Tg(Mpz)88.1Mfel | J:77658 | View | ||||
Charcot-Marie-Tooth disease type 1B | Tg(Mpz)88.2Mfel/0 | FVB/N-Tg(Mpz)88.2Mfel | J:77658 | View | ||||
Charcot-Marie-Tooth disease type 1B | Tg(Mpz)88.4Mfel/0 | FVB/N-Tg(Mpz)88.4Mfel | J:77658 | View | ||||
Charcot-Marie-Tooth disease type 1B | Tg(Mpz*S63X)30Mes/0 | involves: FVB/N | J:105751 | View | ||||
Charcot-Marie-Tooth disease type 1B | Tg(Mpz*S63X)31Mes/0 | involves: FVB/N | J:105751 | View | ||||
Charcot-Marie-Tooth disease type 1C | Litaftm1.1Cwc/Litaftm1.1Cwc | B6.Cg-Litaftm1.1Cwc | J:314784 | View | ||||
Charcot-Marie-Tooth disease type 1E | Pmp22Tr-2J/Pmp22+ | C57BL/6J-Pmp22Tr-2J/GrsrJ | J:201866 | View | ||||
Charcot-Marie-Tooth disease type 2A1 | Kif1btm1Noh/Kif1b+ | involves: 129S4/SvJae * C57BL/6J | J:69772 | View | ||||
Charcot-Marie-Tooth disease type 2A2A | Tg(Mnx1-Mfn2*T105M,-EGFP)1Dcc/Tg(Mnx1-Mfn2*T105M,-EGFP)1Dcc | Not Specified | J:132035 | View | ||||
Charcot-Marie-Tooth disease type 2B | Rab7em2Rwb/Rab7+ | C57BL/6J-Rab7em2Rwb/RwbJ | J:346904 | View | ||||
Charcot-Marie-Tooth disease type 2D | Gars1C201R/Gars1+ | involves: BALB/cAnN * C3H/HeH * C57BL/6J | J:149830, J:179811 | View | ||||
Charcot-Marie-Tooth disease type 2D | Gars1em1Rwb/Gars1em2Rwb | involves: C57BL/6NJ * FVB/NJ | J:284948 | View | ||||
Charcot-Marie-Tooth disease type 2D | Gars1Nmf249/Gars1+ | C57BL/6J-Gars1Nmf249/J | J:112221 | View | ||||
Charcot-Marie-Tooth disease type 2D | Gars1Nmf249/Gars1+ | involves: C57BL/6J * CAST/Ei | J:179811 | View | ||||
Charcot-Marie-Tooth disease type 2E | Nefltm2.1Liem/Nefl+ | B6.Cg-Nefltm2.1Liem | J:220605 | View | ||||
Charcot-Marie-Tooth disease type 3 | Mpztm1Msch/Mpztm1Msch | involves: 129S7/SvEvBrd | J:42838 | View | ||||
Charcot-Marie-Tooth disease type 3 | Pmp22Tr-2J/Pmp22+ | C57BL/6J-Pmp22Tr-2J/GrsrJ | J:201866 | View | ||||
Charcot-Marie-Tooth disease type 3 | Tg(Mpz*S63C)32Mes/0 | involves: FVB/N | J:105751 | View | ||||
Charcot-Marie-Tooth disease type 3 | Tg(Mpz*S63C)33Mes/0 | involves: FVB/N | J:105751 | View | ||||
Charcot-Marie-Tooth disease type 4E | Egr2tm1Jmi/Egr2tm1Jmi | Not Specified | J:96641 | View | ||||
Charcot-Marie-Tooth disease type 4E | Egr2tm2Jmi/Egr2tm2Jmi | B6.Cg-Egr2tm2Jmi | J:145949 | View | ||||
cherubism | Sh3bp2tm1.1Ics/Sh3bp2tm1.1Ics | involves: 129S2/SvPas * C57BL/6 | J:221901 | View | ||||
cherubism | Sh3bp2tm1Bjro/Sh3bp2tm1Bjro | involves: 129S4/SvJae * BALB/cJ * C57BL/6J | J:117880 | View | ||||
CINCA Syndrome | Nlrp3tm3.1Hhf/Nlrp3+ | involves: 129 | J:202147 | View | ||||
cleidocranial dysplasia | Runx2tm1Jals/Runx2tm1Jals | involves: 129S7/SvEvBrd * C57BL/6 | J:143532 | View | ||||
cleidocranial dysplasia | Runx2tm1Kish/Runx2+ | involves: 129P2/OlaHsd * C57BL/6 | J:40783 | View | ||||
cleidocranial dysplasia | Runx2tm1Kish/Runx2tm1Kish | involves: 129P2/OlaHsd * C57BL/6 | J:40783, J:53069, J:54095 | View | ||||
cleidocranial dysplasia | Runx2tm1Mjo/Runx2+ | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:40784, J:53868 | View | ||||
Clouston syndrome | Gjb6tm2.2Kwi/Gjb6tm2.2Kwi | involves: 129P2/OlaHsd * BALB/c * C57BL/6 * CD-1 * SJL | J:208123 | View | ||||
Coffin-Siris syndrome 1 | Arid1bem1Hzhu/Arid1b+ | C57BL/6J-Arid1bem1Hzhu | J:256668 | View | ||||
complex cortical dysplasia with other brain malformations 4 | Tubg1tm1.1Ics/Tubg1+ | involves: C57BL/6N | J:342743 | View | ||||
complex cortical dysplasia with other brain malformations 7 | Tubb2bbrdp/Tubb2bbrdp | involves: A/J * FVB | J:201099 | View | ||||
congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay | Pbx1em1Dunw/Pbx1em1Dunw | C57BL/6J-Pbx1em1Dunw | J:320934 | View | ||||
congenital central hypoventilation syndrome |
Phox2btm1Rth/Phox2b+ Hprt1tm1(CAG-cre)Mnn/? |
involves: 129 * 129S1/Sv * C57BL/6 | J:331513 | View | ||||
congenital central hypoventilation syndrome | Phox2btm2Jbr/Phox2b+ | involves: 129S2/SvPas * C57BL/6 | J:131365 | View | ||||
congenital heart defects, dysmorphic facial features, and intellectual developmental disorder | Cdk13tm1a(EUCOMM)Hmgu/Cdk13tm1a(EUCOMM)Hmgu | involves: C57BL/6N | J:291583 | View | ||||
congenital megabladder | Myocdem1Blk/Myocdtm1.1Msp | involves: 129 | J:283803 | View | ||||
congenital megabladder | Myocdtm1.1Msp/mgb | involves: 129/Sv * FVB/N | J:283803 | View | ||||
congenital muscular dystrophy due to LMNA mutation | Lmnatm2.1Gbon/Lmnatm2.1Gbon | involves: 129 * C57BL/6 | J:180603 | View | ||||
congenital myasthenic syndrome 3A | Tg(Ckm-Chrnd*S262T)40Cgz/0 | involves: C57BL/6 * DBA/2 | J:31221 | View | ||||
congenital myasthenic syndrome 4A | Chrnetm2Vwi/Chrnetm2Vwi | involves: 129P2/OlaHsd * C57BL/6 | J:182046 | View | ||||
congenital myasthenic syndrome 4A | Tg(Ckm-Chrne*L269F)5Cgz/? | involves: FVB/NJ | J:193524 | View | ||||
congenital myopathy 1A | Ryr1m1Nisw/Ryr1+ | 129S1.B6-Ryr1m1Nisw | J:219285 | View | ||||
congenital myopathy 1A | Ryr1tm1.1Dhm/Ryr1+ | involves: 129S2/SvPasCrl * 129S6/SvEvTac | J:155825 | View | ||||
congenital myopathy 1A | Ryr1tm1Tno/Ryr1tm1Tno | involves: 129S4/SvJae * C57BL/6J | J:18895 | View | ||||
congenital stationary night blindness autosomal dominant 1 | Tg(Rho*G90D*A337V)202Sie/0 | involves: C57BL/6 * DBA | J:188632 | View | ||||
congenital stationary night blindness autosomal dominant 2 | Pde6batrd1/Pde6batrd1 | involves: BALB/cAnN * C3H/HeN | J:75964 | View | ||||
congenital stationary night blindness autosomal dominant 2 | Pde6batrd1/Pde6brd1 | involves: BALB/cAnN * C3H/HeN | J:75964 | View | ||||
congenital stationary night blindness autosomal dominant 2 | Pde6batrd2/Pde6batrd2 | involves: BALB/cAnN * C3H/HeN | J:75964 | View | ||||
congenital stationary night blindness autosomal dominant 2 | Pde6batrd2/Pde6brd1 | involves: BALB/cAnN * C3H/HeN | J:75964 | View | ||||
congenital stationary night blindness autosomal dominant 2 | Pde6batrd3/Pde6batrd3 | involves: BALB/cAnN * C3H/HeN | J:75964 | View | ||||
congenital stationary night blindness autosomal dominant 2 | Pde6batrd3/Pde6brd1 | involves: BALB/cAnN * C3H/HeN | J:75964 | View | ||||
congenital stationary night blindness autosomal dominant 2 | Pde6brd1-1H/Pde6brd1 | involves: BALB/cAnN * C3H/HeN | J:75964 | View | ||||
congenital stationary night blindness autosomal dominant 2 | Pde6brd1-2H/Pde6brd1 | involves: BALB/cAnN * C3H/HeN | J:75964 | View | ||||
congenital stationary night blindness autosomal dominant 2 | Pde6brd1-2J/Pde6brd1-2J | C57BL/6J-Pde6brd1-2J/J | J:82238 | View | ||||
congenital stationary night blindness autosomal dominant 2 | Pde6brd1-3H/Pde6brd1-3H | involves: BALB/cAnN * C3H/HeN | J:75964 | View | ||||
congenital stationary night blindness autosomal dominant 2 | Pde6brd1-3H/Pde6brd1 | involves: BALB/cAnN * C3H/HeN | J:75964 | View | ||||
congenital stationary night blindness autosomal dominant 2 | Pde6brd1-4H/Pde6brd1-4H | involves: BALB/cAnN * C3H/HeN | J:75964 | View | ||||
congenital stationary night blindness autosomal dominant 2 | Pde6brd1-4H/Pde6brd1 | involves: BALB/cAnN * C3H/HeN | J:75964 | View | ||||
congenital stationary night blindness autosomal dominant 2 | Pde6brd1/Pde6brd1 | Not Specified | J:24999 | View | ||||
Cornelia de Lange syndrome 1 | NipblGt(RRS564)Byg/Nipbl+ | involves: 129P2/OlaHsd * C57BL/6J * CD-1 | J:297059 | View | ||||
Cornelia de Lange syndrome 1 | NipblGt(RRS564)Byg/Nipbl+ | involves: 129P2/OlaHsd * CD-1 | J:154117 | View | ||||
Cornelia de Lange syndrome 3 | Smc3tm1.2Toshi/Smc3+ | B6.Cg-Smc3tm1.2Toshi | J:242006 | View | ||||
cortisone reductase deficiency 2 | Hsd11b1tm1Yko/Hsd11b1tm1Yko | involves: 129P2/OlaHsd * MF1 | J:37960, J:45085, J:72402 | View | ||||
Costello syndrome |
Hrastm1Jaf/Hras+ Tg(CAG-cre)13Miya/0 |
involves: 129S6/SvEvTac * Black Swiss * C57BL/6 | J:204891 | View | ||||
Costello syndrome | Hrastm2Xbr/Hrastm2Xbr | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N | J:137729 | View | ||||
dentinogenesis imperfecta | Dspptm1Kul/Dspptm1Kul | involves: 129/Sv * C57BL/6 | J:84378 | View | ||||
Denys-Drash syndrome | Wt1tm1.1Lahe/Wt1+ | involves: 129S2/SvPas * C57BL/6 * FVB/NCrl * SJL | J:154995 | View | ||||
Denys-Drash syndrome | Wt1tm1Mlh/Wt1+ | 129P2/OlaHsd-Wt1tm1Mlh | J:135449 | View | ||||
Denys-Drash syndrome | Wt1tm1Mlh/Wt1+ | involves: 129P2/OlaHsd * C57BL/6 | J:135449 | View | ||||
Denys-Drash syndrome | Wt1tm1Mlh/Wt1+ | involves: 129P2/OlaHsd * C57BL/6 * MF1 | J:135449 | View | ||||
Denys-Drash syndrome | Wt1tm1Vih/Wt1+ | involves: 129S7/SvEvBrd * C57BL/6 * MF1 | J:94225 | View | ||||
Denys-Drash syndrome | Wt1tm2Hst/Wt1+ | chimera involves: 129P2/OlaHsd * C57BL/6JLac * CBA/CaLac | J:53585, J:103489 | View | ||||
developmental and epileptic encephalopathy 7 | Kcnq2tm1.1Lvi/Kcnq2+ | 129-Kcnq2tm1.1Lvi/Lvi | J:298666 | View | ||||
developmental and epileptic encephalopathy 14 | Kcnt1em1Lekk/Kcnt1+ | C57BL/6J-Kcnt1em1Lekk | J:287751 | View | ||||
developmental and epileptic encephalopathy 14 | Kcnt1em1Pqt/Kcnt1em1Pqt | C57BL/6J-Kcnt1em1Pqt | J:333512 | View | ||||
developmental and epileptic encephalopathy 17 | Gnao1em1Rneu/Gnao1+ | involves: C57BL/6J * C57BL/6NCrl | J:271137 | View | ||||
developmental and epileptic encephalopathy 17 | Gnao1tm2.1Rneu/Gnao1+ | B6.129S-Gnao1tm2.1Rneu | J:216850 | View | ||||
developmental and epileptic encephalopathy 17 | Gnao1tm2Rneu/Gnao1+ | B6.129S1-Gnao1tm2Rneu | J:271137 | View | ||||
developmental and epileptic encephalopathy 54 | Hnrnpuem1Frk/Hnrnpu+ | Not Specified | J:342579 | View | ||||
Diamond-Blackfan anemia 6 | Rpl5Skax23-Jus/Rpl5+ | 129S6.B6-Rpl5Skax23-Jus | J:330162 | View | ||||
Diamond-Blackfan anemia 7 |
Ndor1Tg(UBC-cre/ERT2)1Ejb/Ndor1+ Rpl11tm1.1Srn/Rpl11+ |
involves: 129S6/SvEvTac * C57BL/6NCrl * CD-1 | J:292575 | View | ||||
DiGeorge syndrome | Del(16Dgcr2-Hira)1Rak/+ | involves: 129/Sv * 129S6/SvEvTac * C57BL/6 * FVB/N * SJL | J:67796 | View | ||||
DiGeorge syndrome | Del(16Dgcr2-Hira)3Aam/+ | involves: 129S7/SvEvBrd | J:141432 | View | ||||
DiGeorge syndrome |
Kat6atm1Avo/Kat6a+ Tbx1tm1Bld/Tbx1+ |
involves: 129 * 129S7/SvEvBrd * BALB/c * C57BL/6 | J:188772 | View | ||||
DiGeorge syndrome |
Nkx2-5tm1(cre)Rjs/Nkx2-5+ Tbx1tm1Bld/Tbx1tm3Bld |
involves: 129S7/SvEvBrd * C57BL/6 | J:91013 | View | ||||
DiGeorge syndrome | Tbx1tm1.1Dsr/Tbx1+ | either: 129/Sv or (involves: 129/Sv * C57BL/6) | J:93588 | View | ||||
DiGeorge syndrome | Tbx1tm1.1Dsr/Tbx1tm1.1Dsr | either: 129/Sv or (involves: 129/Sv * C57BL/6) | J:93588 | View | ||||
DiGeorge syndrome | Tbx1tm1.1Dsr/Tbx1tm1.1Dsr | involves: 129 * C57BL/6J | J:183770, J:217210, J:270507 | View | ||||
DiGeorge syndrome | Tbx1tm1Bem/Tbx1+ | FVB.Cg-Tbx1tm1Bem | J:91664 | View | ||||
DiGeorge syndrome | Tbx1tm1Bem/Tbx1+ | involves: 129/Sv * C57BL/6J * SJL | J:67796 | View | ||||
DiGeorge syndrome | Tbx1tm1Bem/Tbx1tm1Bem | FVB.Cg-Tbx1tm1Bem | J:91664 | View | ||||
DiGeorge syndrome | Tbx1tm1Bld/Tbx1+ | involves: 129S7/SvEvBrd * C57BL/6 | J:67409 | View | ||||
DiGeorge syndrome | Tbx1tm1Bld/Tbx1tm1Bld | involves: 129S7/SvEvBrd * C57BL/6 | J:67409 | View | ||||
DiGeorge syndrome | Tbx1tm1Bld/Tbx1tm2Bld | involves: 129S7/SvEvBrd * C57BL/6 | J:91013 | View | ||||
DiGeorge syndrome |
Tbx1tm1Bld/Tbx1tm3Bld Tg(Myh6-cre)2182Mds/0 |
involves: 129S7/SvEvBrd * C57BL/6 | J:91013 | View | ||||
DiGeorge syndrome |
Tbx1tm1Bld/Tbx1tm3Bld Tg(Tek-cre)1Ywa/0 |
involves: 129S7/SvEvBrd * C57BL/6 | J:91013 | View | ||||
DiGeorge syndrome | Tbx1tm1Dsr/Tbx1+ | either: 129/Sv or (involves: 129/Sv * C57BL/6) | J:93588 | View | ||||
DiGeorge syndrome | Tbx1tm1Dsr/Tbx1tm1Dsr | either: 129/Sv or (involves: 129/Sv * C57BL/6) | J:93588 | View | ||||
DiGeorge syndrome | Tbx1tm1Pa/Tbx1+ | involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ | J:70730 | View | ||||
DiGeorge syndrome | Tbx1tm1Pa/Tbx1+ | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * Swiss Webster | J:70730 | View | ||||
DiGeorge syndrome | Tbx1tm1Pa/Tbx1tm1Pa | either: (involves: 129) or (involves: 129 * C57BL/6) or (involves: 129 * C57BL/6 * Swiss Webster) | J:70730 | View | ||||
DiGeorge syndrome | Tbx1tm1Pa/Tbx1tm1Pa | involves: 129S1/Sv * 129X1/SvJ | J:94411 | View | ||||
DiGeorge syndrome |
Tbx1tm2.1Bem/Tbx1tm2.2Bem Foxg1tm1(cre)Skm/Foxg1+ |
involves: 129 * C57BL/6J * SJL * Swiss Webster | J:105980, J:109536 | View | ||||
DiGeorge syndrome | Tbx1tm2Bld/Tbx1+ | involves: 129S7/SvEvBrd * C57BL/6 | J:91013 | View | ||||
DiGeorge syndrome | Tbx1tm2Bld/Tbx1tm2Bld | involves: 129S7/SvEvBrd * C57BL/6 | J:91013 | View | ||||
dilated cardiomyopathy 1A | Lmnatm1Gbon/Lmnatm1Gbon | involves: 129S2/SvPas * C57BL/6 | J:187399 | View | ||||
dilated cardiomyopathy 1A | Lmnatm1Stw/Lmnatm1Stw | involves: 129S1/Sv | J:87613, J:131905 | View | ||||
dilated cardiomyopathy 1A | Lmnatm2.1Gbon/Lmna+ | involves: 129 * C57BL/6 | J:198526 | View | ||||
dilated cardiomyopathy 1A | Lmnatm3Stw/Lmnatm3Stw | involves: 129S1/Sv * 129S4/SvJaeSor * C57BL | J:100393 | View | ||||
dilated cardiomyopathy 1C |
Ldb3tm4Chen/Ldb3tm4Chen A1cfTg(Myh6-cre/Esr1*)1Jmk/A1cf+ |
involves: 129S1/Sv * 129X1/SvJ * Black Swiss * FVB/N | J:144739 | View | ||||
dilated cardiomyopathy 1C |
Ldb3tm4Chen/Ldb3tm4Chen Myl2tm1(cre)Krc/Myl2+ |
involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * Black Swiss | J:144739 | View | ||||
dilated cardiomyopathy 1CC | Nexnem1Chen/Nexnem1Chen | C57BL/6J-Nexnem1Chen | J:301807 | View | ||||
dilated cardiomyopathy 1CC | Nexntm1.1Chen/Nexntm1.1Chen | Not Specified | J:290931 | View | ||||
dilated cardiomyopathy 1CC |
Nexntm1Chen/Nexntm1Chen Tg(myl7.L-cre)1118Tmhn/0 |
involves: MF1 | J:290931 | View | ||||
dilated cardiomyopathy 1CC |
Nexntm1Chen/Nexntm1Chen Tg(Tnnt2-cre)5Blh/0 |
involves: C57BL/6 * DBA/2 | J:290931 | View | ||||
dilated cardiomyopathy 1D | Tnnt2tm2.1Feah/Tnnt2+ | involves: 129S6/SvEvTac * FVB/N | J:243725 | View | ||||
dilated cardiomyopathy 1D | Tnnt2tm2Mmto/Tnnt2+ | involves: 129S/SvEv * C57BL/6 | J:137784 | View | ||||
dilated cardiomyopathy 1D | Tnnt2tm2Mmto/Tnnt2tm2Mmto | involves: 129S/SvEv * C57BL/6 | J:137784 | View | ||||
dilated cardiomyopathy 1DD | Rbm20em1Hide/Rbm20em1Hide | involves: C57BL/6J | J:297234 | View | ||||
dilated cardiomyopathy 1DD | Rbm20em3Wguo/Rbm20+ | C57BL/6-Rbm20em3Wguo | J:324088 | View | ||||
dilated cardiomyopathy 1DD | Rbm20em3Wguo/Rbm20em3Wguo | C57BL/6-Rbm20em3Wguo | J:324088 | View | ||||
dilated cardiomyopathy 1HH |
Bag3tm1c(EUCOMM)Hmgu/Bag3tm1.1Chen Tg(Myhca-cre)1Abel/0 |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * C57BL/6N * FVB/N | J:246352 | View | ||||
dilated cardiomyopathy 1HH |
Bag3tm1c(EUCOMM)Hmgu/Bag3tm1c(EUCOMM)Hmgu Tg(Myhca-cre)1Abel/0 |
involves: C57BL/6N * FVB/N | J:246352 | View | ||||
dilated cardiomyopathy 1R | Tg(Myh6-Actc1*R312H)307Iko/? | involves: C57BL/6 | J:178587 | View | ||||
dilated cardiomyopathy 1Y | Tg(Myh6-Tpm1*E54K)30Dfw/0 | involves: FVB/N | J:137813 | View | ||||
dilated cardiomyopathy 1Y | Tg(Myh6-Tpm1*E54K)67Dfw/0 | involves: FVB/N | J:137813 | View | ||||
Doyne honeycomb retinal dystrophy | Efemp1tm1Eap/Efemp1+ | involves: 129S6/SvEvTac * C57BL/6 * FVB/N | J:129901 | View | ||||
Doyne honeycomb retinal dystrophy | Efemp1tm1Eap/Efemp1tm1Eap | involves: 129S6/SvEvTac * C57BL/6 * FVB/N | J:129901 | View | ||||
Doyne honeycomb retinal dystrophy | Efemp1tm1Lmar/Efemp1+ | involves: 129X1/SvJ * BALB/c | J:129902 | View | ||||
Doyne honeycomb retinal dystrophy | Efemp1tm1Lmar/Efemp1tm1Lmar | involves: 129X1/SvJ * BALB/c | J:129902 | View | ||||
Dravet syndrome | Scn1atm1.1Kzy/Scn1a+ | involves: 129P2/OlaHsd * C3HeB/FeJ | J:260796 | View | ||||
Dravet syndrome | Scn1atm1Kea/Scn1a+ | (C57BL/6J x 129S6/SvEvTac-Scn1atm1Kea)F1 | J:203040 | View | ||||
Dravet syndrome | Scn1atm1Wac/Scn1a+ | B6.129-Scn1atm1Wac | J:113149, J:188126 | View | ||||
Dravet syndrome | Scn1atm1Wac/Scn1a+ | involves: 129S1/Sv * 129X1/SvJ * FVB/NJ | J:129998 | View | ||||
Dravet syndrome |
Scn1atm2.1Kzy/Scn1a+ Tg(Pvalb-cre)1Tama/0 |
involves: 129P2/OlaHsd * C57BL/6 * DBA | J:202863 | View | ||||
Dravet syndrome |
Scn1atm2.1Kzy/Scn1atm2.1Kzy Tg(Pvalb-cre)1Tama/0 |
involves: 129P2/OlaHsd * C57BL/6 * DBA | J:202863 | View | ||||
Dravet syndrome |
Scn1atm2.1Wac/Scn1a+ Tg(I12b-cre)1Jlr/0 |
involves: 129X1/SvJ * C57BL/6J | J:188126 | View | ||||
Dravet syndrome |
Scn1atm2.1Wac/Scn1a+ Tg(I12b-cre)1Jlr/0 |
involves: C57BL/6J * CD-1 | J:189897 | View | ||||
Duane-radial ray syndrome | Sall4Gt(XE027)Byg/Sall4+ | B6;129P2-Sall4Gt(XE027)Byg | J:105332 | View | ||||
Duane-radial ray syndrome | Sall4Gt(XE027)Byg/Sall4+ | involves: 129P2/OlaHsd * Black Swiss * C57BL/6 | J:105332 | View | ||||
Duane-radial ray syndrome | Sall4tm1Brd/Sall4+ | involves: 129S7/SvEvBrd * C57BL/6J | J:117866 | View | ||||
Duane-radial ray syndrome | Sall4tm1Ryn/Sall4+ | involves: 129P2/OlaHsd * C57BL/6J | J:118119 | View | ||||
ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3 | Trp63tm1Brd/Trp63tm1Brd | involves: 129S7/SvEvBrd * C57BL/6J | J:54636 | View | ||||
ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3 | Trp63tm1Fmc/Trp63tm1Fmc | involves: 129S4/SvJae | J:54637 | View | ||||
ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3 | Trp63tm2Brd/Trp63tm2Brd | involves: 129S7/SvEvBrd * C57BL/6J | J:54636 | View | ||||
ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3 | Trp63tm3Aam/Trp63+ | involves: 129S7/SvEvBrd | J:294158 | View | ||||
Ehlers-Danlos syndrome classic type 1 | Col5a1em1Brle/Col5a1+ | C57BL/6-Col5a1em1Brle | J:326524 | View | ||||
Ehlers-Danlos syndrome classic type 1 | Col5a1tm1Rjw/Col5a1+ | either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * C57BL/6) | J:113133 | View | ||||
Ehlers-Danlos syndrome classic type 1 | Col5a1tm1Rjw/Col5a1+ | involves: 129S6/SvEvTac * C57BL/6 | J:112728, J:326524 | View | ||||
epidermolysis bullosa simplex Ogna type | Plectm1Gwi/Plectm1Gwi | involves: 129S1/Sv * 129X1/SvJ | J:59000 | View | ||||
epidermolysis bullosa simplex Ogna type | Plectm2Gwi/Plectm2Gwi | involves: 129S1/Sv * 129X1/SvJ | J:59000 | View | ||||
epidermolysis bullosa simplex Ogna type | Plectm7.1Gwi/Plec+ | involves: 129P2/OlaHsd * C57BL/6 | J:179812 | View | ||||
epidermolysis bullosa simplex Ogna type | Plectm7.1Gwi/Plectm7.1Gwi | involves: 129P2/OlaHsd * C57BL/6 | J:179812 | View | ||||
episodic kinesigenic dyskinesia 1 | Prrt2tm1d(KOMP)Wtsi/Prrt2+ | B6(Cg)-Prrt2tm1d(KOMP)Wtsi | J:299667 | View | ||||
episodic kinesigenic dyskinesia 1 | Prrt2tm1d(KOMP)Wtsi/Prrt2tm1d(KOMP)Wtsi | B6(Cg)-Prrt2tm1d(KOMP)Wtsi | J:299667 | View | ||||
familial cold autoinflammatory syndrome 1 |
Nlrp3tm2Hhf/Nlrp3+ Lyz2tm1(cre)Ifo/Lyz2+ |
involves: 129/Sv * 129P2/OlaHsd * C57BL/6 | J:150054 | View | ||||
familial cold autoinflammatory syndrome 1 |
Nlrp3tm2Hhf/Nlrp3+ Tg(CAG-cre/Esr1*)5Amc/? |
involves: 129/Sv * C57BL/6 * CBA | J:150054 | View | ||||
familial cold autoinflammatory syndrome 4 | Tg(Cd74-Nlrc4*)1Kyas/0 | involves: C57BL/6N | J:219652 | View | ||||
familial encephalopathy with neuroserpin inclusion bodies | Serpini1tm1Dpw/Serpini1tm1Dpw | involves: 129/Sv * C57BL/6JBom | J:84427 | View | ||||
familial episodic pain syndrome 3 | Scn11aem1Akoi/Scn11a+ | involves: C57BL/6 | J:268684 | View | ||||
familial hyperinsulinemic hypoglycemia 3 |
Gcktm1Ydor/Gck+ Tg(Ins2-cre)25Mgn/0 |
involves: C57BL/6 * C57BL/6J * DBA | J:302600 | View | ||||
familial hypocalciuric hypercalcemia 1 | CasrBCH002/CasrBCH002 | C3HeB/FeJ-CasrBCH002 | J:183993 | View | ||||
familial hypocalciuric hypercalcemia 1 | CasrBCH003/CasrBCH003 | C3HeB/FeJ-CasrBCH003 | J:183993 | View | ||||
familial hypocalciuric hypercalcemia 1 | CasrBCH004/CasrBCH004 | C3HeB/FeJ-CasrBCH004 | J:183993 | View | ||||
familial hypocalciuric hypercalcemia 1 | CasrBCH007/CasrBCH007 | C3HeB/FeJ-CasrBCH007 | J:183993 | View | ||||
familial hypocalciuric hypercalcemia 1 | CasrBCH011/CasrBCH011 | C3HeB/FeJ-CasrBCH011 | J:183993 | View | ||||
familial hypocalciuric hypercalcemia 1 | CasrBCH013/CasrBCH013 | C3HeB/FeJ-CasrBCH013 | J:183993 | View | ||||
familial hypocalciuric hypercalcemia 1 | Casrtm1Ces/Casr+ | involves: 129X1/SvJ * Black Swiss | J:29900 | View | ||||
familial temporal lobe epilepsy 1 | Lgi1tm1.1Ics/Lgi1tm1.1Ics | involves: 129S2/SvPas * BALB/c * C57BL/6 | J:182795 | View | ||||
familial temporal lobe epilepsy 1 |
Lgi1tm1.1Jkc/Lgi1tm1.1Jkc Tyrc-Brd/Tyrc-Brd |
B6.Cg-Tyrc-Brd Lgi1tm1.1Jkc | J:158715 | View | ||||
familial temporal lobe epilepsy 1 | Lgi1tm1Mafu/Lgi1tm1Mafu | involves: 129S6/SvEvTac * C57BL/6 | J:157578 | View | ||||
familial temporal lobe epilepsy 1 | Tg(Lgi1*)#Mpan/0 | Not Specified | J:154129 | View | ||||
fibrodysplasia ossificans progressiva | Acvr1tm1Emsh/Acvr1+ | chimera involves: BALB/c * C57BL/6 * CD-1 | J:194134 | View | ||||
fibrodysplasia ossificans progressiva |
Acvr1tm1Glh/Acvr1+ Gt(ROSA)26Sortm1.2(CAG-EGFP)Glh/Gt(ROSA)26Sor+ Tg(Pdgfra-cre)1Clc/0 |
involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J * FVB/N | J:257905 | View | ||||
fibrodysplasia ossificans progressiva |
Acvr1tm1Glh/Acvr1+ Gt(ROSA)26Sortm1.2(CAG-EGFP)Glh/Gt(ROSA)26Sor+ Tg(Tek-cre)1Ywa/0 |
involves: 129S6/SvEvTac * C57BL/6J * FVB/N * SJL | J:257905 | View | ||||
fibrodysplasia ossificans progressiva |
Acvr1tm2.1Vlcg/Acvr1+ Gt(ROSA)26Sortm3.1(cre/ERT2)Vlcg/Gt(ROSA)26Sor+ |
involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6NTac | J:234069 | View | ||||
fibrodysplasia ossificans progressiva |
Acvr1tm2.1Vlcg/Acvr1+ Tg(Prrx1-cre)1Cjt/0 |
involves: C57BL/6J * C57BL/6NTac * SJL/J | J:239136 | View | ||||
focal segmental glomerulosclerosis 1 | Actn4tm1Mrpk/Actn4tm1Mrpk | involves: 129 * C57BL/6 | J:83911 | View | ||||
focal segmental glomerulosclerosis 2 | Tg(NPHS2-Trpc6)F419Walz/0 | involves: C57BL/6J * CBA/J | J:165112 | View | ||||
focal segmental glomerulosclerosis 2 | Tg(NPHS2-Trpc6*E896K)F75aWalz/0 | involves: C57BL/6J * CBA/J | J:165112 | View | ||||
focal segmental glomerulosclerosis 2 | Tg(NPHS2-Trpc6*P111Q)F615Walz/0 | involves: C57BL/6J * CBA/J | J:165112 | View | ||||
GAND syndrome | Gatad2btm1a(EUCOMM)Hmgu/Gatad2b+ | C57BL/6N-Gatad2btm1a(EUCOMM)Hmgu | J:344365 | View | ||||
gnathodiaphyseal dysplasia | Ano5em1Huyi/Ano5em1Huyi | C57BL/6N-Ano5em1Huyi | J:294237 | View | ||||
gnathodiaphyseal dysplasia | Ano5em2Huyi/Ano5em2Huyi | C57BL/6-Ano5em2Huyi | J:336715 | View | ||||
Greig cephalopolysyndactyly syndrome | Gli3Xt-J/Gli3Xt-J | involves: C3H * CD-1 | J:4086 | View | ||||
Grn-related frontotemporal lobar degeneration with Tdp43 inclusions | Grntm1.1Far/Grntm1.1Far | involves: 129S4/SvJae * C57BL/6J * FVB/N | J:218705 | View | ||||
Grn-related frontotemporal lobar degeneration with Tdp43 inclusions | Grntm1.1Hiok/Grn+ | involves: C57BL/6J | J:259943 | View | ||||
Grn-related frontotemporal lobar degeneration with Tdp43 inclusions | Grntm2.1Far/Grntm2.1Far | involves: 129S4/SvJae * C57BL/6 | J:259651 | View | ||||
Hajdu-Cheney syndrome | Notch2tm1.1Ecan/Notch2+ | involves: 129 * 129S1/Sv * C57BL/6J | J:230045 | View | ||||
Hajdu-Cheney syndrome | Notch2tm1.1Hhtg/Notch2+ | involves: 129S1/Sv * 129X1/SvJ * C57BL/6J | J:311038 | View | ||||
Hajdu-Cheney syndrome |
Notch2tm2.1Ecan/Notch2tm2.1Ecan Tg(BGLAP-cre)1Clem/0 |
involves: C57BL/6J * FVB/NJ | J:246017 | View | ||||
Hajdu-Cheney syndrome | Notch2tm2.2Ecan/Notch2+ | involves: 129S1/Sv * C57BL/6J | J:246017 | View | ||||
hand-foot-genital syndrome | Hoxa13Hd/Hoxa13+ | B6C3Fe-a/a Hoxa13Hd Mcoln3Va-J/J | J:54823 | View | ||||
hand-foot-genital syndrome | Hoxa13Hd/Hoxa13Hd | B6C3Fe-a/a Hoxa13Hd Mcoln3Va-J/J | J:58731 | View | ||||
hand-foot-genital syndrome | Hoxa13Hd/Hoxa13Hd | involves: MYA/Hu | J:64253, J:5211 | View | ||||
hand-foot-genital syndrome | Hoxa13tm1Jwi/Hoxa13+ | involves: 129S7/SvEvBrd | J:94412 | View | ||||
hand-foot-genital syndrome | Hoxa13tm1Jwi/Hoxa13tm1Jwi | involves: 129S7/SvEvBrd | J:94412 | View | ||||
hereditary hemorrhagic telangiectasia | Acvrl1tm1Enl/Acvrl1+ | involves: C57BL/6 | J:82115 | View | ||||
hereditary hemorrhagic telangiectasia |
Acvrl1tm2.1Spo/Acvrl1tm2.1Spo Gt(ROSA)26Sortm1(cre/ERT)Nat/Gt(ROSA)26Sor+ |
involves: 129 * 129S1/Sv * 129X1/SvJ | J:154620 | View | ||||
hereditary hemorrhagic telangiectasia |
Acvrl1tm2.1Spo/Acvrl1tm2.1Spo Tg(Acvrl1-cre)L1Spo/0 |
involves: 129 * FVB | J:154620 | View | ||||
hereditary hemorrhagic telangiectasia |
Acvrl1tm2.1Spo/Acvrl1tm2.1Spo Tg(Tal1-cre/ERT)1Jrg/0 |
involves: 129 * C57BL/6 | J:227170 | View | ||||
hereditary hemorrhagic telangiectasia |
Acvrl1tm2Spo/Acvrl1tm2Spo Tg(Acvrl1-cre)L1Spo/0 |
involves: 129 * 129S4/SvJae * C57BL/6 * FVB/N | J:130020 | View | ||||
hereditary hemorrhagic telangiectasia | Engtm1Dyl/Engtm1Dyl | involves: 129S1/Sv * 129X1/SvJ * C57BL/6J | J:55403 | View | ||||
hereditary hemorrhagic telangiectasia | Engtm1Hma/Eng+ | 129P2/OlaHsd-Engtm1Hma | J:73415 | View | ||||
hereditary hemorrhagic telangiectasia | Engtm1Mle/Eng+ | 129P2/OlaHsd-Engtm1Mle | J:58502 | View | ||||
hereditary hemorrhagic telangiectasia | Engtm1Mle/Eng+ | involves: 129P2/OlaHsd * C57BL/6 | J:58502 | View | ||||
hereditary hemorrhagic telangiectasia |
Engtm2.1Hma/Engtm2.1Hma Gt(ROSA)26Sortm1(cre/ERT)Nat/Gt(ROSA)26Sor+ |
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ | J:212952, J:227170 | View | ||||
hereditary hemorrhagic telangiectasia |
Engtm2.1Hma/Engtm2.1Hma Tg(Tagln-cre)1Her/0 |
involves: 129P2/OlaHsd * C57BL/6 * SJL | J:212952 | View | ||||
hereditary multiple exostoses |
Ext1tm1.1Vcs/Ext1tm1.1Vcs Tg(Col2a1-cre/ERT)KA3Smac/0 |
involves: 129S1/Sv * 129X1/SvJ * FVB/N | J:242977 | View | ||||
hereditary multiple exostoses |
Ext1tm1.1Vcs/Ext1tm1.1Vcs Tg(Col2a1-rtTA,tetO-cre)22Pjro/0 |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL | J:157599 | View | ||||
hereditary multiple exostoses |
Ext1tm1Vcs/Ext1tm1Vcs Tg(Col2a1-rtTA,tetO-cre)22Pjro/0 |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:157599 | View | ||||
hereditary multiple exostoses |
Ext1tm1Yama/Ext1tm1Yama Acantm1(cre/ERT2)Crm/Acan+ |
involves: 129S5/SvEvBrd * 129S6/SvEvTac * C57BL/6NCrl | J:242977 | View | ||||
hereditary multiple exostoses |
Ext1tm1Yama/Ext1tm1Yama Tg(Col2a1-cre/ERT)KA3Smac/0 |
involves: 129S5/SvEvBrd * FVB/N | J:161395 | View | ||||
hereditary neuropathy with liability to pressure palsies | Pmp22tm1Lnot/Pmp22+ | Not Specified | J:104989 | View | ||||
hereditary neuropathy with liability to pressure palsies | Pmp22tm1Ueli/Pmp22tm1Ueli | involves: 129S/SvEv | J:29517 | View | ||||
hereditary neuropathy with liability to pressure palsies | Pmp22Tr-2J/Pmp22+ | C57BL/6J-Pmp22Tr-2J/GrsrJ | J:201866 | View | ||||
hereditary neutrophilia | Csf3rtm1Eur/Csf3rtm1Eur | involves: 129P2/OlaHsd * C57BL/6 * FVB | J:48503 | View | ||||
hereditary spastic paraplegia 4 | SpastM1Gri/SpastM1Gri | B6.C-SpastM1Gri | J:148877 | View | ||||
hereditary spastic paraplegia 4 | Spasttm1.1Evre/Spasttm1.1Evre | C57BL/6-Spasttm1.1Evre | J:253467 | View | ||||
hereditary spastic paraplegia 4 | Spasttm1.1Jme/Spasttm1.1Jme | involves: C57BL/6J | J:117740 | View | ||||
hereditary spastic paraplegia 13 | Hspd1Gt(OST171441)Lex/Hspd1+ | B6.129S5-Hspd1Gt(OST171441)Lex | J:197946 | View | ||||
hereditary spastic paraplegia 31 | Reep1Gt(OST398247)Tigm/Reep1Gt(OST398247)Tigm | B6J.Cg-Reep1Gt(OST398247)Tigm | J:239250 | View | ||||
hereditary spastic paraplegia 80 | Ubap1em1Yta/Ubap1+ | involves: C57BL/6 * C57BL/6N * DBA/2 | J:332139 | View | ||||
hereditary spherocytosis type 1 | Ank1M1Wlst/Ank1M1Wlst | involves: 129S1/SvImJ * C3H/HeJ * C57BL/6 | J:170562 | View | ||||
hereditary spherocytosis type 1 | Ank1nb/Ank1nb | either: (involves: non-inbred stock) or (involves: C57BL/6) or (involves: WB/Re) | J:11441 | View | ||||
hereditary spherocytosis type 1 | Ank1pale/Ank1pale | C57BL/6J-Ank1pale/GrsrJ | J:222308 | View | ||||
hereditary spherocytosis type 1 | Ank1Rbc2/Ank1Rbc2 | involves: 129S1/Sv * BALB/c | J:148127 | View | ||||
holoprosencephaly 2 | Six3tm1Gco/Six3tm1Gco | involves: 129S1/Sv | J:81797 | View | ||||
holoprosencephaly 2 |
Six3tm3.1Gco/Six3+ Shhtm1Chg/Shh+ |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:140315 | View | ||||
holoprosencephaly 2 |
Six3tm3Gco/Six3tm3Gco Foxg1tm1(cre)Skm/Foxg1+ |
involves: 129S1/Sv * C57BL/6 | J:140315 | View | ||||
holoprosencephaly 2 | Six3tm4(cre/ERT2)Gco/Six3+ | involves: 129S1/Sv * C57BL/6 | J:140315 | View | ||||
holoprosencephaly 3 |
Disp1icb/Disp1tm1Amc Shhtm1Amc/Shh+ |
involves: 129X1/SvJ * C57BL/6J | J:92058 | View | ||||
holoprosencephaly 3 | Shhtm1Chg/Shhtm1Chg | involves: 129S1/Sv * 129X1/SvJ | J:35802 | View | ||||
holoprosencephaly 3 | Shhtm1Chg/Shhtm1Chg | involves: C57BL/6 | J:89364 | View | ||||
holoprosencephaly 5 | Zic2Ku/Zic2Ku | 129S.CAnNCrl(C3)-Zic2Ku | J:238567 | View | ||||
holoprosencephaly 5 | Zic2Ku/Zic2Ku | C3.CAnNCrl-Zic2Ku | J:138862 | View | ||||
holoprosencephaly 5 | Zic2tm1Jaru/Zic2tm1Jaru | involves: 129S4/SvJae * C57BL/6 | J:60644 | View | ||||
holoprosencephaly 11 |
Boctm1Rsk/Boc+ Cdontm1Rsk/Cdontm1Rsk |
involves: 129/Sv * 129S6/SvEvTac | J:171767 | View | ||||
holoprosencephaly 11 |
Boctm1Rsk/Boctm1Rsk Cdontm1Rsk/Cdontm1Rsk |
B6.129-Boctm1Rsk Cdontm1Rsk | J:171767 | View | ||||
holoprosencephaly 11 |
Boctm1Rsk/Boctm1Rsk Cdontm1Rsk/Cdontm1Rsk |
involves: 129/Sv * 129S6/SvEvTac | J:171767 | View | ||||
holoprosencephaly 11 |
Boctm2Rsk/Boc+ Cdontm1Rsk/Cdontm1Rsk |
involves: 129/Sv * 129S6/SvEvTac | J:171767 | View | ||||
holoprosencephaly 11 |
Boctm2Rsk/Boctm2Rsk Cdontm1Rsk/Cdontm1Rsk |
B6.129-Boctm2Rsk Cdontm1Rsk | J:171767 | View | ||||
holoprosencephaly 11 |
Boctm2Rsk/Boctm2Rsk Cdontm1Rsk/Cdontm1Rsk |
involves: 129/Sv * 129S6/SvEvTac | J:171767 | View | ||||
holoprosencephaly 11 | Cdontm1Rsk/Cdontm1Rsk | involves: 129/Sv * C57BL/6 | J:82221 | View | ||||
holoprosencephaly 11 | Cdontm2Rsk/Cdontm2Rsk | involves: 129/Sv * C57BL/6 | J:82221 | View | ||||
Holt-Oram syndrome | Tbx5tm1.1Jse/Tbx5+ | either: (involves: 129/Sv) or (involves: Black Swiss) | J:92050, J:112887 | View | ||||
Holt-Oram syndrome | Tbx5tm1.1Jse/Tbx5+ | involves: 129/Sv * Black Swiss | J:71845 | View | ||||
Holt-Oram syndrome | Tbx5tm1Jse/Tbx5+ | involves: 129S/SvEv | J:112887 | View | ||||
hyper IgE recurrent infection syndrome 1 | Tg(Stat3*)9199Alau/0 | involves: C57BL/6 | J:210877 | View | ||||
hyperekplexia 1 | Glra1spd-ot9J/Glra1spd-ot9J | B6.Cg-Glra1spd-ot9J/GrsrJ | J:234690 | View | ||||
hyperekplexia 1 | Glra1spd/Glra1spd | involves: A/HeJ | J:33924 | View | ||||
hyperekplexia 1 | Glra1tm1Betz/Glra1tm1Betz | B6.129P2-Glra1tm1Betz | J:117236 | View | ||||
hyperekplexia 1 | Glra1tm1Rah/Glra1+ | involves: 129X1/SvJ * C57BL/6J | J:85341 | View | ||||
hyperekplexia 3 | Slc6a5tm1Betz/Slc6a5tm1Betz | involves: 129P2/OlaHsd | J:86625 | View | ||||
hyperekplexia 3 | Slc6a5trsl/Slc6a5trsl | C57BL/6J-Slc6a5trsl/GrsrJ | J:235637 | View | ||||
hypochondroplasia | Fgfr3tm3.1Llm/Fgfr3+ | involves: C57BL/6N | J:338859 | View | ||||
hypomyelinating leukodystrophy 6 | Tubb4aem1Avan/Tubb4aem1Avan | involves: C57BL/6 | J:291062 | View | ||||
hypomyelinating leukodystrophy 6 | Tubb4aJit/Tubb4a+ | FVB.B6-Tubb4aJit | J:321692 | View | ||||
hypomyelinating leukodystrophy 6 | Tubb4aJit/Tubb4aJit | FVB.B6-Tubb4aJit | J:321692 | View | ||||
hypotrichosis 13 | Krt71Ca-19J/Krt71+ | BALB/cJ-Krt71Ca-19J/GrsrJ | J:213988 | View | ||||
immunodeficiency 15A | Ikbkbem1Macc/Ikbkb+ | involves: C57BL/6NCrl | J:290616 | View | ||||
immunodeficiency 15A | Ikbkbem1Macc/Ikbkbem1Macc | involves: C57BL/6NCrl | J:290616 | View | ||||
immunodeficiency 73b with defective neutrophil chemotaxis and lymphopenia | Rac2em1Shl/Rac2+ | involves: C57BL/6 | J:276213 | View | ||||
isolated mitochondrial myopathy | Chchd10em3Dpn/Chchd10em3Dpn | C57BL/6J-Chchd10em3Dpn | J:344465 | View | ||||
juvenile polyposis syndrome | Smad4tm1Mmt/Smad4+ | B6.129S2-Smad4tm1Mmt | J:59214 | View | ||||
juvenile polyposis syndrome |
Tg(CAG-Bmpr1a*,-lacZ)1Nobs/0 Tg(Mpz-cre)94Imeg/0 |
involves: 129X1/SvJ * C57BL/6J | J:192670 | View | ||||
KINSSHIP syndrome | Aff3tm1a(EUCOMM)Wtsi/Aff3tm1a(EUCOMM)Wtsi | C57BL/6N-Aff3tm1a(EUCOMM)Wtsi/Wtsi | J:317476 | View | ||||
Kleefstra syndrome 1 |
Ehmt1tm1.1Tara/Ehmt1tm1.1Tara Tg(Camk2a-cre)2Gsc/0 |
involves: 129P2/OlaHsd * C57BL/6 * FVB/N | J:155739 | View | ||||
Kleefstra syndrome 1 | Ehmt1tm1Yshk/Ehmt1+ | involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj | J:157021, J:192316 | View | ||||
Koolen de Vries syndrome | Kansl1em1.1Cya/Kansl1+ | B6(FVB)-Kansl1em1.1Cya | J:327464 | View | ||||
Li-Fraumeni syndrome | Trp53tm1Tyj/Trp53+ | involves: 129S2/SvPas | J:95316 | View | ||||
Li-Fraumeni syndrome | Trp53tm1Tyj/Trp53+ | involves: 129S2/SvPas * C57BL/6 | J:17728 | View | ||||
Li-Fraumeni syndrome | Trp53tm1Tyj/Trp53tm1Tyj | involves: 129S2/SvPas | J:95316 | View | ||||
Li-Fraumeni syndrome | Trp53tm1Tyj/Trp53tm2.1Tyj | involves: 129S2/SvPas * 129S4/SvJae | J:95316 | View | ||||
Li-Fraumeni syndrome | Trp53tm1Tyj/Trp53tm3.1Tyj | involves: 129S2/SvPas * 129S4/SvJae | J:95316 | View | ||||
Li-Fraumeni syndrome | Trp53tm2.1Tyj/Trp53+ | involves: 129S4/SvJae | J:95316 | View | ||||
Li-Fraumeni syndrome | Trp53tm3.1Glo/Trp53+ | B6.129S7-Trp53tm3.1Glo | J:95318 | View | ||||
Li-Fraumeni syndrome | Trp53tm3.1Tyj/Trp53+ | involves: 129S4/SvJae | J:95316 | View | ||||
long QT syndrome 1 | Kcnq1tm3Kpfe/Kcnq1+ | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N | J:93197 | View | ||||
long QT syndrome 3 | Scn5atm1.1Iba/Scn5a+ | involves: 129 * C57BL/6 | J:266290 | View | ||||
long QT syndrome 3 | Scn5atm1Care/Scn5a+ | FVB.129P2-Scn5atm1Care/Care | J:128657 | View | ||||
long QT syndrome 3 | Scn5atm1Clhh/Scn5a+ | involves: 129/SvEv | J:186583 | View | ||||
long QT syndrome 3 | Scn5atm1Pec/Scn5a+ | involves: Swiss | J:71542 | View | ||||
Lynch syndrome |
Apctm1Rak/Apc+ Mlh1tm1Rak/Mlh1tm1Rak |
involves: 129P2/OlaHsd * C57BL/6 | J:53451 | View | ||||
Lynch syndrome | Mlh1tm1Rak/Mlh1tm1Rak | involves: 129P2/OlaHsd * C57BL/6 | J:53451 | View | ||||
Lynch syndrome | Msh2tm1Htr/Msh2tm1Htr | involves: 129P2/OlaHsd | J:45433 | View | ||||
Lynch syndrome |
Msh2tm1Htr/Msh2tm1Htr Tap1tm1Hpl/Tap1tm1Hpl |
involves: 129P2/OlaHsd * FVB | J:45433 | View | ||||
Lynch syndrome |
Msh2tm1Rak/Msh2tm2.1Rak Tg(Vil1-cre)20Syr/0 |
involves: 129/Sv * 129P2/OlaHsd * C57BL/6 * DBA/2 * SJL | J:161577 | View | ||||
Lynch syndrome |
Msh2tm2.1Rak/Msh2tm2.1Rak Tg(Vil1-cre)20Syr/0 |
involves: 129/Sv * C57BL/6 * FVB/N * SJL | J:161577 | View | ||||
Lynch syndrome |
Msh2tm2.1Rak/Msh2tm3.1Rak Tg(Vil1-cre)20Syr/0 |
involves: 129/Sv * C57BL/6 * DBA/2 * SJL | J:161577 | View | ||||
macrocephaly-autism syndrome | Ptentm1Engc/Ptentm1Engc | involves: CD-1 | J:210487 | View | ||||
macrocephaly-autism syndrome |
Ptentm2Mak/Ptentm2Mak Tg(Eno2-cre)39Jme/0 |
involves: 129P2/OlaHsd * C57BL/6 * SJL | J:109635 | View | ||||
malignant hyperthermia | Ryr1em1Tmur/Ryr1+ | Not Specified | J:322211 | View | ||||
malignant hyperthermia | Ryr1tm1Slh/Ryr1+ | involves: 129S7/SvEvBrd * C57BL/6 | J:105738 | View | ||||
malignant hyperthermia | Ryr1tm2.1Alle/Ryr1+ | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:168222 | View | ||||
malignant hyperthermia | Ryr1tm3.1Alle/Ryr1+ | involves: 129 * 129S1/Sv * 129X1/SvJ * C57BL/6 | J:303297 | View | ||||
malignant hyperthermia | Ryr1tm3.1Alle/Ryr1tm3.1Alle | involves: 129 * 129S1/Sv * 129X1/SvJ * C57BL/6 | J:303297 | View | ||||
Marsili syndrome | Tg(Zfhx2*R1907K)#Jcox/0 | involves: C57BL/6 | J:266472 | View | ||||
Marsili syndrome | Zfhx2tm3Ymri/Zfhx2tm3Ymri | involves: 129P2/OlaHsd * C57BL/6 | J:266472 | View | ||||
maturity-onset diabetes of the young type 1 |
Hnf4atm1.1Gonz/Hnf4atm1.1Gonz Tg(Ins2-cre)25Mgn/0 |
involves: 129X1/SvJ * C57BL/6 * DBA | J:108652 | View | ||||
maturity-onset diabetes of the young type 2 | GckGena348/Gck+ | involves: BALB/c * C3H/He | J:90389 | View | ||||
maturity-onset diabetes of the young type 2 | GckGena348/GckGena348 | involves: BALB/c * C3H/He | J:90389 | View | ||||
maturity-onset diabetes of the young type 2 | Gckm1Rge/Gck+ | involves: C3HeB/FeJ | J:162903 | View | ||||
maturity-onset diabetes of the young type 2 | GckRgsc149/Gck+ | involves: C57BL/6J * DBA/2J | J:88919 | View | ||||
maturity-onset diabetes of the young type 2 | GckRgsc210/Gck+ | involves: C57BL/6J * DBA/2J | J:88919 | View | ||||
maturity-onset diabetes of the young type 2 | GckRgsc210/GckRgsc210 | involves: C57BL/6J * DBA/2J | J:88919 | View | ||||
maturity-onset diabetes of the young type 2 | GckRgsc236/Gck+ | involves: C57BL/6J * DBA/2J | J:88919 | View | ||||
maturity-onset diabetes of the young type 2 | GckRgsc272/Gck+ | involves: C57BL/6J * DBA/2J | J:88919 | View | ||||
maturity-onset diabetes of the young type 2 | GckRgsc341/Gck+ | involves: C57BL/6J * DBA/2J | J:88919 | View | ||||
maturity-onset diabetes of the young type 2 | GckRgsc392/Gck+ | involves: C57BL/6J * DBA/2J | J:88919 | View | ||||
maturity-onset diabetes of the young type 2 | GckRgsc392/GckRgsc392 | involves: C57BL/6J * DBA/2J | J:88919 | View | ||||
maturity-onset diabetes of the young type 2 | GckRgsc475/Gck+ | involves: C57BL/6J * DBA/2J | J:88919 | View | ||||
maturity-onset diabetes of the young type 2 | GckRgsc552/Gck+ | involves: C57BL/6J * DBA/2J | J:88919 | View | ||||
maturity-onset diabetes of the young type 2 | GckRgsc553/Gck+ | involves: C57BL/6J * DBA/2J | J:88919 | View | ||||
maturity-onset diabetes of the young type 2 | GckRgsc702/Gck+ | involves: C57BL/6J * DBA/2J | J:88919 | View | ||||
maturity-onset diabetes of the young type 2 | GckRgsc702/GckRgsc702 | involves: C57BL/6J * DBA/2J | J:88919 | View | ||||
maturity-onset diabetes of the young type 2 | GckRgsc735/Gck+ | involves: C57BL/6J * DBA/2J | J:88919 | View | ||||
maturity-onset diabetes of the young type 2 |
Gcktm1.1Mgn/Gck+ Tg(Ins2-cre)25Mgn/0 |
involves: 129S6/SvEvTac * C57BL/6 * DBA/2 | J:51826 | View | ||||
maturity-onset diabetes of the young type 2 |
Gcktm1.1Mgn/Gcktm1.1Mgn Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+ |
involves: 129S6/SvEvTac * C57BL/6 * DBA/2 | J:51826 | View | ||||
maturity-onset diabetes of the young type 2 |
Gcktm1.1Mgn/Gcktm1.1Mgn Tg(Ins2-cre)25Mgn/0 |
involves: 129S6/SvEvTac * C57BL/6 * DBA/2 | J:51826 | View | ||||
maturity-onset diabetes of the young type 2 | Gcktm1.2Mgn/Gck+ | involves: 129S6/SvEvTac * C57BL/6 | J:51826 | View | ||||
maturity-onset diabetes of the young type 2 | Gcktm1.2Mgn/Gcktm1.2Mgn | involves: 129S6/SvEvTac * C57BL/6 | J:51826 | View | ||||
maturity-onset diabetes of the young type 2 | Gcktm1Efr/Gck+ | involves: 129P2/OlaHsd * C57BL/6 | J:28756 | View | ||||
maturity-onset diabetes of the young type 2 |
Gcktm1Hrt/Gck+ Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+ |
involves: C57BL/6 * DBA | J:105247, J:250069 | View | ||||
maturity-onset diabetes of the young type 2 | Gcktm1Tka/Gck+ | involves: 129X1/SvJ * ICR | J:30334 | View | ||||
maturity-onset diabetes of the young type 2 | Gcktm1Ts/Gck+ | either: (involves: 129S7/SvEvBrd * C57BL/6J) or (involves: 129S7/SvEvBrd * DBA/2J) | J:29255 | View | ||||
maturity-onset diabetes of the young type 2 | Gcktm1Ts/Gcktm1Ts | either: (involves: 129S7/SvEvBrd * C57BL/6J) or (involves: 129S7/SvEvBrd * DBA/2J) | J:29255 | View | ||||
maturity-onset diabetes of the young type 2 | Gcktm2Mgn/Gck+ | 129S6/SvEvTac-Gcktm2Mgn | J:121910 | View | ||||
maturity-onset diabetes of the young type 2 | Gcktm2Mgn/Gcktm2Mgn | 129S6/SvEvTac-Gcktm2Mgn | J:121910 | View | ||||
maturity-onset diabetes of the young type 3 | Hnf1atm1.1Ylee/Hnf1atm1.1Ylee | involves: 129X1/SvJ * C57BL/6J | J:47008 | View | ||||
maturity-onset diabetes of the young type 4 | Pdx1tm1Ted/Pdx1+ | involves: 129P2/OlaHsd | J:82969 | View | ||||
mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations | Mast1em1Dak/Mast1+ | B6.Cg-Mast1em1Dak | J:268904 | View | ||||
Mowat-Wilson syndrome | Zeb2tm1.2Yhi/Zeb2tm1.2Yhi | involves: 129S1/Sv * 129X1/SvJ * CD-1 | J:82084 | View | ||||
Muenke Syndrome | Fgfr3tm1.1Aomw/Fgfr3+ | 129S6.129P2-Fgfr3tm1.1Aomw | J:144356 | View | ||||
Muenke Syndrome | Fgfr3tm1.1Aomw/Fgfr3+ | B6.129P2-Fgfr3tm1.1Aomw | J:144356 | View | ||||
Muenke Syndrome | Fgfr3tm1.1Aomw/Fgfr3+ | CBACa.129P2-Fgfr3tm1.1Aomw | J:144356 | View | ||||
Muenke Syndrome | Fgfr3tm1.1Aomw/Fgfr3tm1.1Aomw | 129S6.129P2-Fgfr3tm1.1Aomw | J:144356 | View | ||||
Muenke Syndrome | Fgfr3tm1.1Aomw/Fgfr3tm1.1Aomw | B6.129P2-Fgfr3tm1.1Aomw | J:144356 | View | ||||
Muenke Syndrome | Fgfr3tm1.1Aomw/Fgfr3tm1.1Aomw | CBACa.129P2-Fgfr3tm1.1Aomw | J:144356 | View | ||||
multicentric carpotarsal osteolysis syndrome | Mafbem1Staka/Mafbem1Staka | involves: C57BL/6J | J:279108 | View | ||||
multiple endocrine neoplasia type 1 | Men1tm1.1Gfk/Men1+ | involves: 129T2/SvEms * C57BL/6 | J:116086 | View | ||||
multiple endocrine neoplasia type 1 |
Men1tm1.2Zqw/Men1tm1.2Zqw Tg(Ins2-cre)23Herr/0 |
involves: 129P2/OlaHsd * C57BL/6J * CBA/J | J:85133 | View | ||||
multiple endocrine neoplasia type 1 |
Men1tm1Ctre/Men1tm1Ctre Tg(Pdx1-cre)89.1Dam/0 |
involves: 129S6/SvEvTac * C57BL/6 * CBA * FVB/N | J:146440 | View | ||||
multiple endocrine neoplasia type 1 |
Men1tm1Gfk/Men1tm1Gfk Tg(Ins2-cre)25Mgn/0 |
involves: 129T2/SvEms * C57BL/6 * C57BL/6J * DBA | J:89898 | View | ||||
multiple endocrine neoplasia type 1 | Men1tm1Rvt/Men1+ | involves: 129 * C57BL/6 | J:191261 | View | ||||
multiple endocrine neoplasia type 1 | Men1tm1Zqw/Men1+ | involves: 129/Sv * 129P2/OlaHsd | J:85302 | View | ||||
multiple endocrine neoplasia type 1 | Men1tm2.1Gfk/Men1+ | involves: 129T2/SvEms * C57BL/6 | J:116086 | View | ||||
multiple endocrine neoplasia type 2B | Rettm2.1Cos/Ret+ | involves: 129S1/Sv * C57BL/6J * FVB/N | J:60659 | View | ||||
multiple endocrine neoplasia type 2B | Rettm2.1Cos/Rettm2.1Cos | involves: 129S1/Sv * C57BL/6J * FVB/N | J:60659 | View | ||||
multiple epiphyseal dysplasia 5 | Matn3tm1Mbri/Matn3tm1Mbri | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:125104 | View | ||||
myoclonic dystonia 11 | Sgcetm1Ygl/Sgce+ | involves: 129S2/SvPas | J:180682 | View | ||||
myoclonic dystonia 11 | Sgcetm1Ygl/Sgcetm1Ygl | involves: 129S2/SvPas * 129S4/SvJaeSor * BALB/c * C57BL/6 | J:101332 | View | ||||
myofibrillar myopathy 1 | Destm1.1Ccrs/Des+ | involves: 129 * C57BL/6J | J:219616 | View | ||||
myofibrillar myopathy 1 | Destm1.1Ccrs/Destm1.1Ccrs | involves: 129 * C57BL/6J | J:219616 | View | ||||
myofibrillar myopathy 1 | Destm1Cap/Destm1Cap | involves: 129S7/SvEvBrd * C57BL/6 | J:35123 | View | ||||
myofibrillar myopathy 1 | Tg(Myh6-Des*)641Rbns/0 | involves: FVB/N | J:108730 | View | ||||
myofibrillar myopathy 2 | Cryabtm1.1Ady/Cryab+ | involves: 129X1/SvJ * C57BL/6 * C57BL/6J | J:171679 | View | ||||
myofibrillar myopathy 2 | Cryabtm1.1Ady/Cryabtm1.1Ady | involves: 129X1/SvJ * C57BL/6 * C57BL/6J | J:171679 | View | ||||
myofibrillar myopathy 2 | Tg(Myh6-Cryab*R120G)708Rbns/0 | FVB/N-Tg(Myh6-Cryab*R120G)708Rbns | J:133093 | View | ||||
myofibrillar myopathy 2 | Tg(Myh6-CRYAB*R120G)7302Ijb/0 | involves: C57BL/6 | J:126781 | View | ||||
myofibrillar myopathy 5 | Flnctm1.1Rsdf/Flnc+ | involves: C57BL/6 | J:226976 | View | ||||
nail-patella syndrome | Lmx1btm1Rjo/Lmx1btm1Rjo | involves: 129 * C57BL/6 | J:47316 | View | ||||
nail-patella syndrome | Lmx1btm1Rjo/Lmx1btm1Rjo | involves: 129S7/SvEvBrd | J:95961 | View | ||||
nail-patella syndrome | Lmx1btm1Rjo/Lmx1btm1Rjo | involves: 129S7/SvEvBrd * C57BL/6 | J:95961 | View | ||||
nail-patella syndrome |
Lmx1btm4.1Rjo/Lmx1btm4.1Rjo Tg(NPHS2-cre)295Lbh/0 |
involves: 129S7/SvEvBrd * C57BL/6 * SJL | J:122505 | View | ||||
nemaline myopathy 6 | Kbtbd13em1Coeo/Kbtbd13em1Coeo | involves: C57BL/6J | J:295442 | View | ||||
neurodevelopmental disorder with dysmorphic facies and distal limb anomalies |
Bptftm1.1Cwu/Bptftm1.1Cwu Emx1tm1(cre)Krj/Emx1+ |
involves: 129S1/Sv * 129S2/SvPas * C57BL/6 | J:334252 | View | ||||
neurodevelopmental disorder with involuntary movements | Gnao1em2Rneu/Gnao1+ | C57BL/6J-Gnao1em2Rneu | J:303229 | View | ||||
neurofibromatosis 1 |
Grin1tm1Stl/Grin1+ Nf1tm1Tyj/Nf1+ |
involves: 129S2/SvPas * C57BL/6J | J:38703 | View | ||||
neurofibromatosis 1 | Nf1Mhdadsk9/Nf1+ | involves: C3HeB/FeJ * C57BL/6 | J:269534 | View | ||||
neurofibromatosis 1 |
Nf1tm1.1Kest/Nf1tm1c(KOMP)Wtsi Tg(Dhh-cre)1Mejr/0 |
involves: 129S4/SvJaeSor * C57BL/6 * C57BL/6N * C57BL/6NTac * FVB/N | J:234172 | View | ||||
neurofibromatosis 1 |
Nf1tm1c(KOMP)Wtsi/Nf1tm1c(KOMP)Wtsi Tg(Dhh-cre)1Mejr/0 |
involves: 129S4/SvJaeSor * C57BL/6 * C57BL/6N * FVB/N | J:234172 | View | ||||
neurofibromatosis 1 | Nf1tm1Cbr/Nf1tm1Cbr | involves: 129S1/Sv * C57BL/6 | J:68489 | View | ||||
neurofibromatosis 1 |
Nf1tm1Fcr/Nf1+ Trp53tm1Tyj/Trp53+ |
involves: 129S/SvEv * 129S2/SvPas * C57BL/6 | J:58877 | View | ||||
neurofibromatosis 1 | Nf1tm1Fcr/Nf1tm1Fcr | either: (involves: 129S/SvEv) or (involves: 129S/SvEv * C57BL/6J) | J:18048 | View | ||||
neurofibromatosis 1 |
Nf1tm1Par/Nf1tm1Fcr Tg(GFAP-cre)#Gtm/0 |
involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA | J:165209 | View | ||||
neurofibromatosis 1 |
Nf1tm1Par/Nf1tm1Par H2az2Tg(Wnt1-cre)11Rth/H2az2+ |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA | J:80323 | View | ||||
neurofibromatosis 1 |
Nf1tm1Par/Nf1tm1Par Tg(Fabp7-cre,-lacZ)3Gtm/0 |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA | J:138868 | View | ||||
neurofibromatosis 1 |
Nf1tm1Par/Nf1tm1Par Tg(Mpz-cre)94Imeg/0 |
involves: 129S1/Sv * 129X1/SvJ | J:80323 | View | ||||
neurofibromatosis 1 |
Nf1tm1Par/Nf1tm1Par Tg(Pax3-cre)1Joe/0 |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL | J:80323 | View | ||||
neurofibromatosis 1 |
Nf1tm1Par/Nf1tm1Par Tg(Prrx1-cre)1Cjt/0 |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * C57BL/6N * SJL/J | J:193350 | View | ||||
neurofibromatosis 1 |
Nf1tm1Par/Nf1tm1Par Tg(Prrx1-cre)1Cjt/0 |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SJL/J | J:173779 | View | ||||
neurofibromatosis 1 |
Nf1tm1Par/Nf1tm1Par Tg(Syn1-cre)671Jxm/0 |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA | J:68558 | View | ||||
neurofibromatosis 1 | Nf1tm1Tyj/Nf1+ | involves: 129S2/SvPas * C57BL/6J | J:38703 | View | ||||
neurofibromatosis 1 |
Nf1tm1Tyj/Nf1+ Trp53tm1Tyj/Trp53+ |
involves: 129/Sv * C57BL/6 | J:58876 | View | ||||
neurohypophyseal diabetes insipidus | Avptm1Hari/Avp+ | involves: 129S1/Sv * 129X1/SvJ * C57BL/6J | J:147993 | View | ||||
neurohypophyseal diabetes insipidus | Avptm1Lja/Avp+ | involves: 129S1/Sv * 129X1/SvJ | J:148012 | View | ||||
Noonan syndrome 1 |
Emx1tm1(cre)Krj/Emx1+ Ptpn11tm6Bgn/Ptpn11+ |
B6.129S-Ptpn11tm6Bgn Emx1tm1(cre)Krj | J:242312 | View | ||||
Noonan syndrome 1 | Ptpn11tm1Bgn/Ptpn11+ | involves: 129S4/SvJae * C57BL/6J | J:91609 | View | ||||
Noonan syndrome 1 | Tg(Myh7-Ptpn11*Q79R)11Rbns/0 | FVB.Cg-Tg(Myh7-Ptpn11*Q79R)11Rbns | J:123963 | View | ||||
Noonan syndrome 3 | Krastm4.1Bbd/Krastm4.1Bbd | involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * C57BL/6J * FVB/N | J:223433 | View | ||||
Noonan syndrome 4 | Sos1tm1.2Rak/Sos1+ | involves: 129S/Sv * C57BL/6 * FVB/N * SJL | J:171873 | View | ||||
Noonan syndrome 4 | Sos1tm1.2Rak/Sos1tm1.2Rak | involves: 129S/Sv * C57BL/6 * FVB/N * SJL | J:171873 | View | ||||
Noonan syndrome 5 | Raf1tm1.1Bgn/Raf1+ | involves: 129S6/SvEvTac * C57BL/6NCr | J:172034 | View | ||||
Noonan syndrome 5 | Raf1tm2.1Ara/Raf1tm2.1Ara | involves: 129S6/SvEvTac * C57BL/6NCr | J:189143 | View | ||||
Noonan syndrome 8 | Rit1tm1.1Tumg/Rit1+ | B6.Cg-Rit1tm1.1Tumg | J:277548 | View | ||||
Noonan syndrome 10 | Lztr1tm1a(EUCOMM)Wtsi/Lztr1+ | involves: C57BL/6N | J:268690 | View | ||||
osteogenesis imperfecta type 1 | Col1a1Mov13/Col1a1+ | involves: C57BL/6 | J:107045 | View | ||||
osteogenesis imperfecta type 2 | Col1a1Aga2/Col1a1+ | involves: C3HeB/FeJ * C57BL/6J | J:129569 | View | ||||
osteogenesis imperfecta type 2 | Col1a1tm1Jcm/Col1a1+ | either: (involves: 129X1/SvJ * C3H/HeJ) or (involves: 129X1/SvJ * CD-1) | J:59168 | View | ||||
osteogenesis imperfecta type 3 | Col1a1Aga2/Col1a1+ | C3HeB/FeJ-Col1a1Aga2 | J:185988 | View | ||||
osteogenesis imperfecta type 3 | Col1a2oim/Col1a2oim | B6C3Fe a/a-Col1a2oim/J | J:38013 | View | ||||
osteogenesis imperfecta type 3 | Col1a2oim/Col1a2oim | involves: C3H/HeJ * C57BL/6JLe | J:4348 | View | ||||
osteogenesis imperfecta type 4 | Col1a1M1Jrt/Col1a1+ | involves: C3H/HeJ * C57BL/6J * FVB/NJ | J:216423 | View | ||||
osteogenesis imperfecta type 4 | Col1a1M1Jrt/Col1a1+ | involves: C57BL/6 * FVB/N | J:228439 | View | ||||
osteogenesis imperfecta type 4 | Col1a1tm1.1Jcm/Col1a1+ | either: (involves: 129X1/SvJ * C3H/HeJ) or (involves: 129X1/SvJ * CD-1) | J:59168 | View | ||||
osteogenesis imperfecta type 5 | Tg(Col1a1-Ifitm5*)1Brle/0 | involves: FVB/N | J:233366 | View | ||||
pachyonychia congenita | Krt16tm1(KOMP)Vlcg/Krt16tm1(KOMP)Vlcg | C57BL/6-Krt16tm1(KOMP)Vlcg | J:184621 | View | ||||
Pallister-Hall syndrome | Gli3tm1Urt/Gli3tm1Urt | involves: 129P2/OlaHsd * C57BL/6 | J:76496 | View | ||||
palmoplantar keratoderma-esophageal carcinoma syndrome | Rhbdf2cub/Rhbdf2cub | B6.Cg-Rhbdf2cub | J:250259 | View | ||||
palmoplantar keratoderma-esophageal carcinoma syndrome | Rhbdf2cub/Rhbdf2cub | MRL.Cg-Rhbdf2cub | J:250259 | View | ||||
palmoplantar keratoderma-esophageal carcinoma syndrome | Rhbdf2em2Mvw/Rhbdf2em2Mvw | C57BL/6J-Rhbdf2em2Mvw/Mvw | J:244160 | View | ||||
Parkinson's disease 1 | Sncatm1.1Koks/Snca+ | either: B6.129P2-Sncatm1.1Koks or (involves: 129P2/OlaHsd * C57BL/6) | J:201391 | View | ||||
Parkinson's disease 1 |
Sncatm1Nbm/Sncatm1Nbm Tg(SNCA*A30P)1Nbm/Tg(SNCA*A30P)1Nbm Tg(SNCA*A30P)2Nbm/Tg(SNCA*A30P)2Nbm |
involves: 129S6/SvEvTac * FVB/N | J:156741 | View | ||||
Parkinson's disease 1 |
Sncatm1Nbm/Sncatm1Nbm Tg(SNCA*A53T)1Nbm/Tg(SNCA*A53T)1Nbm Tg(SNCA*A53T)2Nbm/Tg(SNCA*A53T)2Nbm |
involves: 129S6/SvEvTac * FVB/N | J:156741 | View | ||||
Parkinson's disease 1 | Sncatm1Rosl/Sncatm1Rosl | involves: 129X1/SvJ * C57BL/6 | J:60151 | View | ||||
Parkinson's disease 1 |
Sncatm1Rosl/Sncatm1Rosl Tg(SNCA)OVX37Rwm/0 |
B6.Cg-Tg(SNCA)OVX37Rwm Sncatm1Rosl | J:201991 | View | ||||
Parkinson's disease 1 |
Sncatm1Rosl/Sncatm1Rosl Tg(SNCA*A30P)192Rwm/0 |
B6.Cg-Sncatm1Rosl Tg(SNCA*A30P)#Rwm | J:201961 | View | ||||
Parkinson's disease 4 | Tg(Thy1-Snca)1S13Putt/? | involves: C57BL/6 | J:177661 | View | ||||
Parkinson's disease 8 | Tg(Lrrk2*G2019S)2Yue/0 | involves: C3H * C57BL/6 * C57BL/6J | J:157931 | View | ||||
Parkinson's disease 17 | Vps35Gt(RRK261)Byg/Vps35+ | B6.129P2-Vps35Gt(RRK261)Byg | J:225806 | View | ||||
Parkinson's disease 17 | Vps35tm1.1Hlw/Vps35+ | involves: 129S/SvEv * C57BL/6J | J:329507 | View | ||||
paroxysmal nonkinesigenic dyskinesia 1 | Tg(Pnkd*A7V*A9V,-DsRed)671Ljp/0 | B6.Cg-Tg(Pnkd*A7V*A9V,-DsRed)671Ljp | J:192798 | View | ||||
paroxysmal nonkinesigenic dyskinesia 1 | Tg(Pnkd*A7V*A9V,-DsRed)704Ljp/0 | B6.Cg-Tg(Pnkd*A7V*A9V,-DsRed)704Ljp | J:192798 | View | ||||
PCWH syndrome | Sox10gt/Sox10gt | GT/Le | J:216967 | View | ||||
Pelger-Huet anomaly | Lbric-J/Lbric-J | involves: 129S4/SvJae * C57BL/6 | J:143838 | View | ||||
permanent neonatal diabetes mellitus |
Gt(ROSA)26Sortm1(CAG-Kcnj11*,-GFP)Nich/Gt(ROSA)26Sor+ Tg(Ins2-cre)23Herr/0 |
involves: C57BL/6 * CBA/J | J:146650 | View | ||||
permanent neonatal diabetes mellitus |
Gt(ROSA)26Sortm1(Kcnj11*V59M)Fmas/Gt(ROSA)26Sor+ Tg(Ins2-cre)23Herr/0 |
involves: 129S4/SvJae * C57BL/6 | J:144715 | View | ||||
permanent neonatal diabetes mellitus |
Gt(ROSA)26Sortm1(Kcnj11*V59M)Fmas/Gt(ROSA)26Sor+ Tg(Nes-cre)1Kln/0 |
involves: 129S4/SvJae * C57BL/6 * SJL | J:162008 | View | ||||
permanent neonatal diabetes mellitus | Ins2Akita/Ins2Akita | C57BL/6-Ins2Akita | J:47883 | View | ||||
Pfeiffer syndrome | Fgfr1tm1Led/Fgfr1tm1Led | involves: 129S4/SvJae * NIH Black Swiss | J:22118 | View | ||||
Pfeiffer syndrome | Fgfr1tm2.1Cxd/Fgfr1+ | D2.129S6(Cg)-Fgfr1tm2.1Cxd | J:228708 | View | ||||
Pfeiffer syndrome | Fgfr2tm2.3Dsn/Fgfr2+ | involves: 129 * C57BL/6 * FVB/N | J:72517 | View | ||||
piebaldism | KitWps/KitWps | involves: C57BL/6J * CBA/CaJ | J:196572 | View | ||||
Pierpont syndrome | Tbl1xr1em2H/Tbl1xr1em2H | C57BL/6J-Tbl1xr1em2H | J:335355 | View | ||||
Pitt-Hopkins syndrome | Tcf4em1Bdph/? | involves: C57BL/6 * C57BL/6J | J:254983 | View | ||||
Pitt-Hopkins syndrome | Tcf4em2Bdph/? | involves: C57BL/6 * C57BL/6J | J:254983 | View | ||||
Pitt-Hopkins syndrome | Tcf4tm1a(EUCOMM)Wtsi/Tcf4+ | involves: C57BL/6N | J:265025 | View | ||||
Pitt-Hopkins syndrome |
Tcf4tm1Hmb/Tcf4+ Tg(Nes-cre)1Kln/0 |
involves: 129P2/OlaHsd * C57BL/6 * SJL | J:254983 | View | ||||
Pitt-Hopkins syndrome |
Tcf4tm1Hmb/Tcf4+ Tmem163Tg(ACTB-cre)2Mrt/Tmem163+ |
involves: 129P2/OlaHsd * C57BL/6 * FVB/N | J:254983 | View | ||||
Pitt-Hopkins syndrome | Tcf4tm1Zhu/Tcf4+ | involves: 129P2/OlaHsd * 129S1/SvImJ * C57BL/6J | J:239016 | View | ||||
platelet-type bleeding disorder 16 | Itga2btm1Tlr/Itga2btm1Tlr | either: (involves: 129S1/Sv * 129X1/SvJ * BALB/c) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) | J:63961 | View | ||||
platelet-type bleeding disorder 16 | Itgb3tm1Hyn/Itgb3tm1Hyn | involves: 129S2/SvPas * C57BL/6 | J:52262 | View | ||||
polycystic kidney disease 1 |
Gpsm1tm1.1Lajb/Gpsm1tm1.1Lajb Pkd1tm1.1Fqi/Pkd1tm1.1Fqi |
involves: 129S6/SvEvTac | J:193175 | View | ||||
polycystic kidney disease 1 | Pkd1b2b1585Clo/Pkd1b2b1585Clo | C57BL/6J-Pkd1b2b1585Clo | J:175213 | View | ||||
polycystic kidney disease 1 | Pkd1tm1.1Fqi/Pkd1tm1.1Fqi | involves: 129S6/SvEvTac | J:193175 | View | ||||
polycystic kidney disease 1 | Pkd1tm1.1Pcha/Pkd1tm1.1Pcha | involves: 129S1/Sv * C57BL/6 | J:193544 | View | ||||
polycystic kidney disease 1 |
Pkd1tm1.1Pcha/Pkd1tm2Som Tg(Cdh16-cre)91Igr/0 |
involves: 129 * 129S4/SvJae * C57BL/6 * ICR | J:244067 | View | ||||
polycystic kidney disease 1 | Pkd1tm1Bdgz/Pkd1+ | involves: 129S1/Sv * 129X1/SvJ | J:130086 | View | ||||
polycystic kidney disease 1 | Pkd1tm1Djmp/Pkd1tm1Djmp | involves: 129P2/OlaHsd * C57BL/6 | J:94582 | View | ||||
polycystic kidney disease 1 | Pkd1tm1Ggg/Pkd1tm1Ggg | Not Specified | J:76062 | View | ||||
polycystic kidney disease 1 |
Pkd1tm1Gztn/Pkd1tm1Gztn Gt(ROSA)26Sortm9(cre/ESR1)Arte/Gt(ROSA)26Sor+ |
involves: 129S/Sv * 129S7/SvEvBrd * C57BL/6 | J:162080 | View | ||||
polycystic kidney disease 1 | Pkd1tm1Jzh/Pkd1+ | either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c) | J:43193, J:52573, J:72627 | View | ||||
polycystic kidney disease 1 | Pkd1tm1Jzh/Pkd1tm1Jzh | either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c) | J:43193, J:72627, J:81443 | View | ||||
polycystic kidney disease 1 | Pkd1tm1Rsa/Pkd1+ | involves: 129S4/SvJaeSor | J:72238 | View | ||||
polycystic kidney disease 1 | Pkd1tm1Shh/Pkd1tm1.1Pcha | involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6 | J:193544 | View | ||||
polycystic kidney disease 1 |
Pkd1tm1Som/Pkd1+ Tg(Pkd1*)39Mtru/0 |
involves: 129/Sv * C57BL/6J * CBA/J * SJL | J:198147 | View | ||||
polycystic kidney disease 1 | Pkd1tm2.1Ggg/Pkd1tm2.1Ggg | involves: 129S4/SvJae * Black Swiss * C57BL/6 | J:103719 | View | ||||
polycystic kidney disease 1 |
Pkd1tm2Ggg/Pkd1tm2Ggg Tg(Col1a1-cre)1Bek/0 |
involves: 129S4/SvJae * CD-1 | J:191967 | View | ||||
polycystic kidney disease 1 |
Pkd1tm2Ggg/Pkd1tm2Ggg Tg(Hoxb7-cre)13Amc/0 |
involves: 129S4/SvJae * C57BL/6 | J:171619 | View | ||||
polycystic kidney disease 1 |
Pkd1tm2Ggg/Pkd1tm2Ggg Tg(MMTV-cre)4Mam/0 |
involves: 129S4/SvJae * FVB | J:103719 | View | ||||
polycystic kidney disease 1 |
Pkd1tm2Ggg/Pkd1tm2Ggg Tg(Nes-cre)Wme/0 |
involves: 129S4/SvJae * C57BL/6 * CBA | J:185855 | View | ||||
polycystic kidney disease 1 | Pkd1tm2Jzh/Pkd1+ | either: (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6) | J:72627 | View | ||||
polycystic kidney disease 1 | Pkd1tm2Jzh/Pkd1tm2Jzh | either: (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6) | J:72627 | View | ||||
polycystic kidney disease 1 | Pkd1tm2Jzh/Pkd1tm2Jzh | involves: 129S4/SvJae * C57BL/6 | J:140012 | View | ||||
polycystic kidney disease 1 |
Pkd1tm2Som/Pkd1tm2.1Som Tg(Cdh16-cre)91Igr/0 |
involves: C57BL/6 * ICR * SJL | J:135301 | View | ||||
polycystic kidney disease 1 |
Pkd1tm2Som/Pkd1tm2Som Tg(Cdh16-cre)91Igr/0 |
involves: 129S4/SvJae * C57BL/6 * ICR | J:244067 | View | ||||
polycystic kidney disease 1 | Pkd1tm3.1Jzh/Pkd1tm3.1Jzh | involves: 129P2/OlaHsd * C57BL/6 | J:140012 | View | ||||
polycystic kidney disease 1 |
Pkd1tm3Jzh/Pkd1tm3Jzh Tg(Ggt1-cre)M3Egn/0 |
involves: 129P2/OlaHsd * C57BL/6 * SJL | J:140012 | View | ||||
polycystic kidney disease 1 | Tg(Pkd1*)39Mtru/0 | involves: C57BL/6J * CBA/J | J:198147 | View | ||||
polycystic kidney disease 2 | Pkd2tm1Dwo/Pkd2tm1Dwo | either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) | J:77401 | View | ||||
polycystic kidney disease 2 | Pkd2tm1Som/Pkd2+ | involves: 129/Sv * C57BL/6J * SJL | J:47035 | View | ||||
polycystic kidney disease 2 | Pkd2tm1Som/Pkd2tm1Som | involves: 129/Sv * C57BL/6J * SJL | J:47035 | View | ||||
polycystic kidney disease 2 | Pkd2tm1Som/Pkd2tm2Som | involves: 129/Sv * C57BL/6J * SJL | J:47035 | View | ||||
polycystic kidney disease 2 | Pkd2tm2Som/Pkd2+ | involves: 129/Sv * C57BL/6J * SJL | J:59314 | View | ||||
polycystic kidney disease 2 | Pkd2tm2Som/Pkd2tm2Som | involves: 129/Sv * C57BL/6J * SJL | J:59314 | View | ||||
polycystic kidney disease 2 |
Pkd2tm3Som/Pkd2tm3Som Tg(Pkhd1-cre)1Igr/0 |
involves: 129S4/SvJae * C57BL/6 | J:244067 | View | ||||
popliteal pterygium syndrome | Irf6Gt(OST398253)Lex/Irf6Gt(OST398253)Lex | involves: 129S5/SvEvBrd * C57BL/6 | J:115343 | View | ||||
popliteal pterygium syndrome | Irf6tm1Mjd/Irf6+ | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:116077 | View | ||||
progeria | LmnaDhe/Lmna+ | B6(D2)-LmnaDhe/TyGrsrJ | J:171665 | View | ||||
progeria | Lmnaem1Fenz/Lmna+ | C57BL/6-Lmnaem1Fenz | J:338760 | View | ||||
progeria | Lmnatm1.1Bliu/Lmna+ | involves: C57BL/6 * FVB/N | J:287256 | View | ||||
progeria | Lmnatm1.1Bliu/Lmnatm1.1Bliu | involves: C57BL/6 * FVB/N | J:287256 | View | ||||
progeria | Lmnatm1.1Otin/Lmna+ | involves: 129P2/OlaHsd * C57BL/6 | J:211388 | View | ||||
progeria | Lmnatm1.1Otin/Lmna+ | involves: 129P2/OlaHsd * C57BL/6NTac | J:261974 | View | ||||
progeria |
Lmnatm1.1Otin/Lmna+ Nat10tm1a(KOMP)Wtsi/Nat10+ |
involves: 129P2/OlaHsd * C57BL/6NTac | J:261974 | View | ||||
progeria | Lmnatm1.1Otin/Lmnatm1.1Otin | involves: 129P2/OlaHsd * C57BL/6 | J:177575, J:177632, J:211388 | View | ||||
progeria | Lmnatm1.1Otin/Lmnatm1.1Otin | involves: 129P2/OlaHsd * C57BL/6NTac | J:261974 | View | ||||
progeria |
Lmnatm1.1Otin/Lmnatm1.1Otin Nat10tm1a(KOMP)Wtsi/Nat10+ |
involves: 129P2/OlaHsd * C57BL/6NTac | J:261974 | View | ||||
progeria |
Lmnatm1Bliu/Lmnatm1Bliu Tg(Tek-cre)1Ywa/0 |
involves: C57BL/6 * SJL | J:287256 | View | ||||
progeria | Lmnatm1Lgf/Lmna+ | involves: 129P2/OlaHsd * C57BL/6 | J:113119 | View | ||||
progeria | Lmnatm2Stw/Lmnatm2Stw | involves: 129S1/Sv | J:83382 | View | ||||
progeria | Lmnatm12Lgf/Lmnatm12Lgf | involves: 129P2/OlaHsd * C57BL/6 | J:234711 | View | ||||
progressive familial heart block type IA | Scn5atm1Agrc/Scn5a+ | involves: 129 | J:109689 | View | ||||
progressive familial heart block type IA | Scn5atm1Agrc/Scn5a+ | involves: 129 * C57BL/6J | J:76331 | View | ||||
pseudoachondroplasia | Comptm1Mbri/Comptm1Mbri | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:125086 | View | ||||
pseudoachondroplasia | Comptm2.1Mbri/Comptm2.1Mbri | involves: 129S1/Sv * 129X1/SvJ | J:206511 | View | ||||
renal coloboma syndrome | Pax21Neu/Pax2+ | involves: 102 * CD-1 | J:145105 | View | ||||
renal coloboma syndrome | Pax2M1Bpb/Pax2+ | C57BL/6-Pax2M1Bpb | J:159240 | View | ||||
renal coloboma syndrome | Pax2M1Bpb/Pax2M1Bpb | C57BL/6-Pax2M1Bpb | J:159240 | View | ||||
renal coloboma syndrome | Pax2tm1Pgr/Pax2+ | involves: 129S1/Sv * 129X1/SvJ | J:36834 | View | ||||
renal coloboma syndrome | Pax2tm1Pgr/Pax2tm1Pgr | involves: 129S1/Sv * 129X1/SvJ | J:36834 | View | ||||
renal coloboma syndrome | Pax2tm1Pgr/Pax2tm1Pgr | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:92326 | View | ||||
retinitis pigmentosa 1 | Rp1m1Jdun/Rp1m1Jdun | C57BL/6-Rp1m1Jdun | J:214837 | View | ||||
retinitis pigmentosa 1 | Rp1tm1Jnz/Rp1tm1Jnz | involves: 129S7/SvEvBrd | J:76071 | View | ||||
retinitis pigmentosa 4 | RhoR3/Rho+ | C57BL/6J-RhoR3 | J:153281 | View | ||||
retinitis pigmentosa 4 | RhoR3/RhoR3 | C57BL/6J-RhoR3 | J:153281 | View | ||||
retinitis pigmentosa 4 | RhoR3/Rhotm1Jlem | involves: 129S4/SvJae * C57BL/6J | J:153281 | View | ||||
retinitis pigmentosa 4 | Rhotm1.1Eye/Rho+ | involves: 129S6/SvEvTac * C57BL/6 | J:205477 | View | ||||
retinitis pigmentosa 4 | Rhotm1.1Kpal/Rho+ | involves: 129S6/SvEvTac * C57BL/6 * FVB/N | J:170648 | View | ||||
retinitis pigmentosa 4 |
Rhotm1Jlem/Rhotm1Jlem Tg(RHO*P347S)A1Tili/0 |
involves: 129S4/SvJae * FVB/N | J:280289 | View | ||||
retinitis pigmentosa 4 | Rhotm1Phm/Rhotm1Phm | involves: 129S1/Sv * 129X1/SvJ | J:38098 | View | ||||
retinitis pigmentosa 4 | Rhotm2(RHO/GFP)Jhw/Rhotm2(RHO/GFP)Jhw | involves: 129S7/SvEvBrd | J:128212 | View | ||||
retinitis pigmentosa 4 | Rhotm4.1(RHO*/EGFP)Jhw/Rho+ | B6.129S7-Rhotm4.1(RHO*/EGFP)Jhw | J:196863 | View | ||||
retinitis pigmentosa 4 | RhoTvrm1/Rho+ | C57BL/6J-RhoTvrm1 | J:159523 | View | ||||
retinitis pigmentosa 4 | RhoTvrm4/Rho+ | B6.Cg-RhoTvrm4/Pjn | J:159523 | View | ||||
retinitis pigmentosa 4 | RhoTvrm334/Rho+ | B6.Cg-RhoTvrm334/Pjn | J:243745 | View | ||||
retinitis pigmentosa 4 | Tg(Rho)1Wbae/0 | involves: C57BL/6 * SJL | J:12791 | View | ||||
retinitis pigmentosa 7 | Prph2Rd2/Prph2+ | either: (involves: BALB/c * O20/A) or (involves: GR/A * O20/A) or (involves: O20/A * STS/A) | J:25582 | View | ||||
retinitis pigmentosa 7 | Prph2tm1Nmc/Prph2+ | involves: 129S1/Sv * 129X1/SvJ | J:76490 | View | ||||
retinitis pigmentosa 7 | Prph2tm1Nmc/Prph2tm1Nmc | involves: 129S1/Sv * 129X1/SvJ | J:76490 | View | ||||
retinitis pigmentosa 11 | Prpf31tm1.1Bha/Prpf31+ | involves: 129S2/SvPas | J:171561 | View | ||||
retinitis pigmentosa 13 | Prpf8tm1.1Eap/Prpf8+ | involves: 129S6/SvEvTac * C57BL/6 * SJL | J:171561 | View | ||||
retinitis pigmentosa 13 | Prpf8tm1.1Eap/Prpf8tm1.1Eap | involves: 129S6/SvEvTac * C57BL/6 * SJL | J:171561 | View | ||||
retinitis pigmentosa 18 | Prpf3tm1.1Eap/Prpf3+ | involves: 129S6/SvEvTac * C57BL/6 * SJL | J:171561 | View | ||||
retinitis pigmentosa 18 | Prpf3tm1.1Eap/Prpf3tm1.1Eap | involves: 129S6/SvEvTac * C57BL/6 * SJL | J:171561 | View | ||||
rippling muscle disease 2 | Cav3tm1Mls/Cav3tm1Mls | involves: 129/Sv * C57BL/6J * SJL | J:69965 | View | ||||
rippling muscle disease 2 | Cav3tm1Ncnp/Cav3tm1Ncnp | involves: 129S4/SvJae * C57BL/10 | J:150127 | View | ||||
rippling muscle disease 2 | Tg(Ckmm-Cav3)1Ysu/0 | involves: C57BL/Slc * DBA/Slc | J:67174 | View | ||||
Rubinstein-Taybi syndrome | CrebbpGt(U-San)112Imeg/Crebbp+ | involves: C57BL/6 * CBA | J:53370 | View | ||||
Rubinstein-Taybi syndrome |
Crebbptm1.2Ltz/Crebbptm1.2Ltz Tg(Camk2a-cre)T29-1Stl/0 |
involves: 129P2/OlaHsd * BALB/c * C57BL * C57BL/6J | J:168984 | View | ||||
Rubinstein-Taybi syndrome | Crebbptm1Dli/Crebbp+ | involves: 129S6/SvEvTac * C57BL/6 | J:60630 | View | ||||
Rubinstein-Taybi syndrome | Crebbptm1Sis/Crebbp+ | involves: C57BL/6NCrlj * CBA/JNCrlj | J:42932 | View | ||||
Saethre-Chotzen syndrome |
Msx2tm1Rilm/Msx2+ Twist1tm1Bhr/Twist1+ |
involves: 129S4/SvJae * 129S7/SvEvBrd * BALB/c * C57BL/6 | J:87044 | View | ||||
Saethre-Chotzen syndrome | Twist1Pas/Twist1+ | involves: C57BL/6 * PDT/Pas | J:86815 | View | ||||
Saethre-Chotzen syndrome | Twist1Pas/Twist1Pas | involves: C57BL/6 * PDT/Pas | J:86815 | View | ||||
Saethre-Chotzen syndrome | Twist1Pde/Twist1+ | involves: 129S1/Sv * C57BL/6J | J:69450 | View | ||||
Saethre-Chotzen syndrome | Twist1Pde/Twist1Pde | involves: 129S1/Sv * C57BL/6J | J:69450 | View | ||||
Saethre-Chotzen syndrome | Twist1tm1Bhr/Twist1+ | involves: 129S1/Sv * 129X1/SvJ * C57BL/6J | J:79294 | View | ||||
Saethre-Chotzen syndrome | Twist1tm1Bhr/Twist1+ | involves: 129S7/SvEvBrd * C57BL/6 | J:44379 | View | ||||
Saethre-Chotzen syndrome | Twist1tm1Bhr/Twist1tm1Bhr | involves: 129S7/SvEvBrd * C57BL/6 | J:44379 | View | ||||
scalp-ear-nipple syndrome |
Kctd1tm1c(EUCOMM)Wtsi/Kctd1tm1c(EUCOMM)Wtsi Kctd15tm1c(EUCOMM)Wtsi/Kctd15tm1c(EUCOMM)Wtsi Tg(KRT14-cre)1Amc/0 |
involves: C57BL/6N * C57BL/6NJ | J:344153 | View | ||||
scalp-ear-nipple syndrome |
Kctd1tm1c(EUCOMM)Wtsi/Kctd1tm1c(EUCOMM)Wtsi Tg(Six2-EGFP/cre)1Amc/0 |
involves: C57BL/6J * C57BL/6N * CD-1 | J:344153 | View | ||||
Schnyder corneal dystrophy | Ubiad1em1Wwk/Ubiad1+ | C57BL/6N-Ubiad1em1Wwk | J:268574 | View | ||||
Schnyder corneal dystrophy | Ubiad1em1Wwk/Ubiad1em1Wwk | C57BL/6N-Ubiad1em1Wwk | J:268574 | View | ||||
sclerosteosis 2 | Lrp4mdig-3J/Lrp4mdig-3J | B6.Cg-Lrp4mdig-3J/GrsrJ | J:224655 | View | ||||
sclerosteosis 2 | Lrp4tm1.1Pg/Lrp4tm1.1Pg | involves: C57BL/6N | J:277372 | View | ||||
SHORT syndrome | Pik3r1tm1.1Geno/Pik3r1+ | involves: C57BL/6 * C57BL/6J | J:234657 | View | ||||
Sorsby's fundus dystrophy | Timp3tm1Web/Timp3+ | either: (involves: 129/Sv) or (involves: 129/Sv * C57BL/6) | J:78059 | View | ||||
Sorsby's fundus dystrophy | Timp3tm1Web/Timp3tm1Web | either: (involves: 129/Sv) or (involves: 129/Sv * C57BL/6) | J:78059 | View | ||||
Sotos syndrome 2 | Nfixtm1.1Rmg/Nfix+ | involves: 129S4/SvJae * C57BL/6J | J:295051 | View | ||||
spinocerebellar ataxia type 1 | Atxn1tm1Hzo/Atxn1+ | involves: 129S7/SvEvBrd * C57BL/6 | J:77225 | View | ||||
spinocerebellar ataxia type 2 | Atxn2tm2.1Aub/Atxn2tm2.1Aub | B6.129S2-Atxn2tm2.1Aub | J:188118 | View | ||||
spinocerebellar ataxia type 5 | Sptbn2Gt(XK442)Byg/Sptbn2Gt(XK442)Byg | involves: 129P2/OlaHsd * C57BL/6J | J:158494 | View | ||||
spinocerebellar ataxia type 5 | Sptbn2tm1Mjac/Sptbn2tm1Mjac | B6.129P2-Sptbn2tm1Mjac | J:159622 | View | ||||
spinocerebellar ataxia type 6 | Cacna1asmrl/Cacna1asmrl | CXB10/HiAJ-Cacna1asmrl/GrsrJ | J:222308 | View | ||||
spinocerebellar ataxia type 6 | Cacna1atm2.1Kewa/Cacna1atm2.1Kewa | B6.Cg-Cacna1atm2.1Kewa | J:190729 | View | ||||
spinocerebellar ataxia type 6 | Cacna1atm3Hzo/Cacna1atm3Hzo | B6.129S7-Cacna1atm3Hzo/J | J:239981 | View | ||||
spinocerebellar ataxia type 7 | Atxn7tm1Hzo/Atxn7+ | involves: 129S7/SvEvBrd | J:113150, J:179021 | View | ||||
spinocerebellar ataxia type 7 | Atxn7tm1Hzo/Atxn7+ | involves: 129S7/SvEvBrd * C57BL/6 | J:82072 | View | ||||
spinocerebellar ataxia type 7 | Atxn7tm1Hzo/Atxn7+ | involves: 129S7/SvEvBrd * C57BL/6J | J:107098 | View | ||||
spinocerebellar ataxia type 7 | Atxn7tm1Hzo/Atxn7tm1Hzo | involves: 129S7/SvEvBrd | J:179021 | View | ||||
spinocerebellar ataxia type 7 |
Atxn7tm1Hzo/Atxn7tm1Hzo Kat2atm3.1Roth/Kat2a+ |
involves: 129 * 129S7/SvEvBrd | J:179021 | View | ||||
spinocerebellar ataxia type 14 | Prkcgem1Jpka/Prkcg+ | FVB/N-Prkcgem1Jpka | J:305637 | View | ||||
spinocerebellar ataxia type 14 | Prkcgem1Jpka/Prkcgem1Jpka | FVB/N-Prkcgem1Jpka | J:305637 | View | ||||
spinocerebellar ataxia type 17 |
Tbptm1Xjl/Tbp+ Tg(CAG-cre/Esr1*)5Amc/0 |
involves: 129S/SvEv * C57BL/6 * CBA | J:213011 | View | ||||
spinocerebellar ataxia type 28 | Afg3l2Emv66/Afg3l2+ | involves: MEV/2Ty | J:151797 | View | ||||
split hand-foot malformation 1 | Del(6Dlx6-Dlx5)1Tlu/Del(6Dlx6-Dlx5)1Tlu | Not Specified | J:76480 | View | ||||
split hand-foot malformation 1 | Dlx5/Dlx6tm1Levi/Dlx5/Dlx6tm1Levi | Not Specified | J:77244 | View | ||||
spondyloepiphyseal dysplasia congenita | Col2a1Lpk/Col2a1+ | C.B6(C3)-Col2a1Lpk | J:187141 | View | ||||
spondyloepiphyseal dysplasia congenita | Col2a1Lpk/Col2a1+ | involves: C3H/HeH * C57BL/6J | J:187141 | View | ||||
spondyloepiphyseal dysplasia congenita | Col2a1M2J/Col2a1+ | B6;C3Fe-Col2a1M2J/GrsrJ | J:222308 | View | ||||
spondyloepiphyseal dysplasia congenita | Col2a1M3J/Col2a1+ | B6(Cg)-Col2a1M3J/GrsrJ | J:222308 | View | ||||
spondyloepiphyseal dysplasia congenita | Col2a1sedc/Col2a1sedc | involves: C57BL/6J | J:85735 | View | ||||
spondyloepiphyseal dysplasia congenita | Col2a1tm1Prc/Col2a1tm1Prc | involves: 129/Sv * C57BL/6 | J:30041 | View | ||||
spondyloepiphyseal dysplasia congenita | Tg(Col2a1*R789C)#Waho/0 | involves: C57BL/6 * DBA/2 | J:112540 | View | ||||
STING-associated vasculopathy with onset in infancy | Sting1em1Jmin/Sting1+ | involves: C57BL/6N | J:251372 | View | ||||
Stormorken syndrome | Stim1tm3Ics/Stim1+ | involves: C57BL/6N | J:277842, J:327797 | View | ||||
Teebi hypertelorism syndrome 1 | Specc1lem3Kumc/Specc1lem3Kumc | involves: C57BL/6J * FVB/NJ | J:324294 | View | ||||
Teebi hypertelorism syndrome 1 | Specc1lem4Kumc/Specc1lem4Kumc | involves: C57BL/6J * FVB/NJ | J:324294 | View | ||||
tibial muscular dystrophy | Ttntm1.1Isrd/Ttn+ | involves: 129S2/SvPas * C57BL/6 | J:165576 | View | ||||
Tietz syndrome | MitfMi-Crc/Mitf+ | involves: CBA/CaCrc | J:83500 | View | ||||
Tietz syndrome | MitfMi-Crc/MitfMi-Crc | involves: CBA/CaCrc | J:83500 | View | ||||
Tietz syndrome | Mitfmi-enu122/Mitf+ | involves: 102 * C3H | J:46254 | View | ||||
Tietz syndrome | Mitfmi-enu122/Mitfmi-enu122 | involves: 102 * C3H | J:46254 | View | ||||
Tietz syndrome | MitfMi-H/Mitf+ | involves: BALB/cAnN * C3H/HeN | J:75964 | View | ||||
Tietz syndrome | MitfMi-H/MitfMi-H | involves: BALB/cAnN * C3H/HeN | J:75964 | View | ||||
Tietz syndrome | MitfMi-H/MitfRorp | involves: BALB/cAnN * C3H/HeN | J:75964 | View | ||||
Tietz syndrome | MitfMi-wh/Mitf+ | involves: C57BL * DBA | J:13058 | View | ||||
Tietz syndrome | MitfMi-wh/MitfMi-wh | involves: C57BL * DBA | J:13058 | View | ||||
Tietz syndrome | MitfMi-wh/Mitfmi-x | involves: NZB/Mac | J:83501 | View | ||||
Tietz syndrome | Mitfmi-x/Mitfmi-x | involves: NZB/Mac | J:83501 | View | ||||
Tietz syndrome | MitfMi/MitfMi | Not Specified | J:30758 | View | ||||
Tietz syndrome | MitfRorp/Mitf+ | involves: BALB/cAnN * C3H/HeN | J:75964 | View | ||||
Tietz syndrome | MitfRorp/MitfRorp | involves: BALB/cAnN * C3H/HeN | J:75964 | View | ||||
Timothy syndrome | Cacna1ctm2Itl/Cacna1c+ | involves: 129S6/SvEvTac * C57BL/6J * C57BL/6NTac | J:176442 | View | ||||
TNF receptor associated periodic syndrome | Tnfrsf1atm1Imx/Tnfrsf1atm1Imx | involves: 129S7/SvEvBrd * C57BL/6 | J:45147 | View | ||||
TNF receptor associated periodic syndrome | Tnfrsf1atm1Rsie/Tnfrsf1a+ | B6.Cg-Tnfrsf1atm1Rsie | J:160543 | View | ||||
TNF receptor associated periodic syndrome | Tnfrsf1atm2.1Rsie/Tnfrsf1a+ | B6.Cg-Tnfrsf1atm2.1Rsie | J:160543 | View | ||||
torsion dystonia 1 | Tor1atm1Wtd/Tor1a+ | B6;129-Tor1atm1Wtd/J | J:225496 | View | ||||
torsion dystonia 1 | Tor1atm1Yql/Tor1a+ | involves: 129S2/SvPas * C57BL/6 | J:104513 | View | ||||
torsion dystonia 1 | Tor1atm2Wtd/Tor1a+ | B6.129S1-Tor1atm2Wtd | J:171370, J:201962 | View | ||||
torsion dystonia 1 | Tor1atm2Wtd/Tor1a+ | involves: 129S1/Sv | J:201535 | View | ||||
torsion dystonia 6 | Thap1tm1.1Meeh/Thap1+ | involves: 129S/SvEv * C3H * C57BL/6 | J:226849 | View | ||||
torsion dystonia 6 | Thap1tm1.2Meeh/Thap1+ | involves: 129S/SvEv * BALB/cJ * C3H * C57BL/6 | J:226849 | View | ||||
Townes-Brocks syndrome | Sall1tm1.1Mrau/Sall1+ | involves: 129X1/SvJ | J:161758 | View | ||||
Townes-Brocks syndrome | Sall1tm1Mrau/Sall1+ | involves: 129X1/SvJ * ICR | J:85458 | View | ||||
Townes-Brocks syndrome | Sall1tm1Mrau/Sall1tm1Mrau | involves: 129X1/SvJ * ICR | J:85458 | View | ||||
transthyretin amyloidosis |
Rbp4tm1(RBP4)Zhel/Rbp4tm1(RBP4)Zhel Ttrtm2(TTR)Kymm/Ttrtm2(TTR)Kymm |
B6.Cg-Ttrtm2(TTR)Kymm Rbp4tm1(RBP4)Zhel | J:260683 | View | ||||
transthyretin amyloidosis |
Rbp4tm1(RBP4)Zhel/Rbp4tm1(RBP4)Zhel Ttrtm2(TTR)Kymm/Ttrtm3(TTR*)Kymm |
Not Specified | J:260683 | View | ||||
transthyretin amyloidosis | Tg(TTR)#Jbux/0 | involves: C57BL/6 * DBA/2 | J:68458 | View | ||||
transthyretin amyloidosis | Ttrtm1.1Smoc/? | involves: C57BL/6J * C57BL/6N | J:257096 | View | ||||
Treacher Collins syndrome | Tcof1tm1Mjd/Tcof1+ | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:62928 | View | ||||
Treacher Collins syndrome | Tcof1tm1Mjd/Tcof1+ | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/1 | J:112900 | View | ||||
trichorhinophalangeal syndrome type I | Trps1tm1.1Shiv/Trps1+ | either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6) | J:80615 | View | ||||
tuberous sclerosis |
Myl2tm1(cre)Krc/Myl2+ Tsc1tm1Djk/Tsc1tm1Djk |
involves: 129S4/SvJae | J:96138 | View | ||||
tuberous sclerosis | Tg(CMV-Tsc2*)1Arbi/0 | involves: C57BL/6 | J:96943, J:179850 | View | ||||
tuberous sclerosis |
Tg(GFAP-cre)8Gtm/0 Tsc2tm1.1Mjg/Tsc2tm1.1Mjg |
involves: 129X1/SvJ * 129S1/Sv * C57BL/6 * CBA | J:167241 | View | ||||
tuberous sclerosis |
Tg(Pcp2-cre)2Mpin/0 Tsc2tm1.1Mjg/Tsc2tm1.1Mjg |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J | J:174327 | View | ||||
tuberous sclerosis |
Tg(Pcp2-cre)2Mpin/0 Tsc2tm1.1Mjg/Tsc2tm1.2Mjg |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J | J:174327 | View | ||||
tuberous sclerosis | Tsc1tm1.1Djk/Tsc1+ | either: 129S4/SvJae-Tsc1tm1Djk or (involves: 129S4/SvJae * BALB/cJ) or (involves: 129S4/SvJae * C57BL/6J) | J:75243 | View | ||||
tuberous sclerosis | Tsc1tm1Chdl/Tsc1+ | involves: 129P2/OlaHsd * Balb/cOlaHsd * C57BL/6JOlaHsd | J:99796 | View | ||||
tuberous sclerosis | Tsc1tm1Chdl/Tsc1+ | involves: 129P2/OlaHsd * C3H/HeNHsd * C57BL/6JOlaHsd | J:99796 | View | ||||
tuberous sclerosis | Tsc1tm1Chdl/Tsc1+ | involves: 129P2/OlaHsd * C57BL/6JOlaHsd | J:99796 | View | ||||
tuberous sclerosis |
Tsc1tm1Djk/Tsc1tm1.1Djk Tg(Syn1-cre)671Jxm/0 |
involves: 129S4/SvJae * C57BL/6 * CBA | J:136366 | View | ||||
tuberous sclerosis |
Tsc1tm1Djk/Tsc1tm1Djk Gt(ROSA)26Sortm1Sho/Gt(ROSA)26Sor+ |
involves: 129S4/SvJae * 129S4/SvJaeSor | J:221022 | View | ||||
tuberous sclerosis |
Tsc1tm1Djk/Tsc1tm1Djk Tg(GFAP-cre)8Gtm/0 |
involves: 129S4/SvJae * C57BL/6 * CBA | J:134889, J:167241 | View | ||||
tuberous sclerosis | Tsc1tm1Hin/Tsc1+ | B6J.129S4-Tsc1tm1Hin | J:221239 | View | ||||
tuberous sclerosis | Tsc1tm1Hin/Tsc1+ | involves: 129S4/SvJae * C57BL/6J | J:70463 | View | ||||
tuberous sclerosis | Tsc2tm1Djk/Tsc2+ | either: (involves: 129S4/SvJae * BALB/cJ) or (involves: 129S4/SvJae * Black Swiss) or (involves: 129S4/SvJae * C57BL/6J) | J:57631 | View | ||||
tuberous sclerosis | Tsc2tm1Djk/Tsc2+ | involves: 129S4/SvJae * C57BL/6NCrl | J:138621 | View | ||||
tuberous sclerosis | Tsc2tm1Tno/Tsc2+ | B6J.129S4-Tsc2tm1Tno | J:221239 | View | ||||
tuberous sclerosis | Tsc2tm1Tno/Tsc2+ | involves: 129S4/SvJae * C57BL/6J | J:52464 | View | ||||
tuberous sclerosis | Tsc2tm2.2Djk/Tsc2+ | involves: 129S4/SvJae * C57BL/6 | J:149326 | View | ||||
tubular aggregate myopathy 1 | Stim1tm1.1Pg/Stim1+ | involves: C57BL/6 | J:285187 | View | ||||
tubular aggregate myopathy 1 | Stim1tm3Ics/Stim1+ | involves: C57BL/6N | J:277842, J:327797 | View | ||||
ulnar-mammary syndrome | Tbx3tm1Pa/Tbx3tm1Pa | either: (involves: 129 * 129S1/Sv * 129X1/SvJ) or (involves: 129 * 129S1/Sv * 129X1/SvJ * C57BL/6NTac) | J:82458 | View | ||||
vascular type Ehlers-Danlos syndrome | Col3a1m1Lsmi/Col3a1+ | involves: 129P2/OlaHsd * C57BL/6J | J:180733 | View | ||||
vascular type Ehlers-Danlos syndrome | Col3a1tm1Jae/Col3a1tm1Jae | involves: 129S4/SvJae | J:39273 | View | ||||
vestibular schwannomatosis |
Nf2tm2Gth/Nf2tm2Gth Tg(Postn-cre)1Sjc/0 |
involves: 129P2/OlaHsd * FVB/NTac | J:216420 | View | ||||
Waardenburg syndrome type 1 | Pax3Sp-1Wli/Pax3+ | involves: C57BL/6J * CBA/CaJ | J:196572 | View | ||||
Waardenburg syndrome type 1 | Pax3Sp-2H/Pax3+ | involves: C57BL/6 | J:14096 | View | ||||
Waardenburg syndrome type 1 | Pax3Sp-2H/Pax3Sp-2H | involves: 101 * C3H/He * CBA/Ca | J:46341 | View | ||||
Waardenburg syndrome type 1 | Pax3Sp-2H/Pax3Sp-2H | involves: C57BL/6 | J:14096 | View | ||||
Waardenburg syndrome type 1 | Pax3Sp-d/Pax3+ | C57BL/6J-Pax3Sp-d | J:238 | View | ||||
Waardenburg syndrome type 1 | Pax3Sp-d/Pax3Sp-d | C57BL/6J-Pax3Sp-d | J:238, J:70476 | View | ||||
Waardenburg syndrome type 2A |
Mitfmi-bw/Mitfmi-bw Tg(Dct-lacZ)A12Jkn/0 |
involves: C3H * C57BL/6 * C57BL/6J * CBA | J:213982 | View | ||||
Waardenburg syndrome type 2A | MitfMi-Crc/MitfMi-Crc | involves: CBA/CaCrc | J:83500 | View | ||||
Waardenburg syndrome type 2A | Mitfmi-enu122/Mitf+ | involves: 102 * C3H | J:46254 | View | ||||
Waardenburg syndrome type 2A | Mitfmi-enu122/Mitfmi-enu122 | involves: 102 * C3H | J:46254 | View | ||||
Waardenburg syndrome type 2A | MitfMi-H/Mitf+ | involves: BALB/cAnN * C3H/HeN | J:75964 | View | ||||
Waardenburg syndrome type 2A | MitfMi-H/MitfMi-H | involves: BALB/cAnN * C3H/HeN | J:75964 | View | ||||
Waardenburg syndrome type 2A | MitfMi-H/MitfRorp | involves: BALB/cAnN * C3H/HeN | J:75964 | View | ||||
Waardenburg syndrome type 2A | MitfMi-wh/Mitf+ | involves: C57BL * DBA | J:13058 | View | ||||
Waardenburg syndrome type 2A | MitfMi-wh/MitfMi-wh | involves: C57BL * DBA | J:13058 | View | ||||
Waardenburg syndrome type 2A | MitfMi-wh/Mitfmi-x | involves: NZB/Mac | J:83501 | View | ||||
Waardenburg syndrome type 2A | Mitfmi-x/Mitfmi-x | involves: NZB/Mac | J:83501 | View | ||||
Waardenburg syndrome type 2A | MitfMi/MitfMi | Not Specified | J:30758 | View | ||||
Waardenburg syndrome type 2A | MitfRorp/Mitf+ | involves: BALB/cAnN * C3H/HeN | J:75964 | View | ||||
Waardenburg syndrome type 2A | MitfRorp/MitfRorp | involves: BALB/cAnN * C3H/HeN | J:75964 | View | ||||
Waardenburg syndrome type 4A | Ednrbtm1Ywa/Ednrbtm1Ywa | involves: 129S5/SvEvBrd | J:93622 | View | ||||
Waardenburg syndrome type 4A | EdnrbWS4/EdnrbWS4 | involves: BALB/c * MSM | J:76584 | View | ||||
Waardenburg syndrome type 4B | Edn3tm1Ywa/Edn3tm1Ywa | involves: 129S7/SvEvBrd | J:22207 | View | ||||
Waardenburg syndrome type 4B | Edn3tmgc48/Edn3+ | C57BL/6-19PWK | J:137432 | View | ||||
Waardenburg syndrome type 4B | Edn3tmgc48/Edn3tmgc48 | C57BL/6-19PWK | J:137432 | View | ||||
Waardenburg syndrome type 4C | Sox10Dom/Sox10+ | C57BL/6J-Sox10Dom | J:165146 | View | ||||
Weaver syndrome | Ezh2em1Jbn/Ezh2+ | C57BL/6J-Ezh2em1Jbn | J:267184 | View | ||||
Weaver syndrome | Ezh2em1Jbn/Ezh2em1Jbn | C57BL/6J-Ezh2em1Jbn | J:267184 | View | ||||
Weaver syndrome | Ezh2em1Jiaf/Ezh2+ | C57BL/6J-Ezh2em1Jiaf | J:345603 | View | ||||
WHIM syndrome 1 | Cxcr4tm1.1Bala/Cxcr4+ | B6.129S2-Cxcr4tm1.1Bala | J:186735 | View | ||||
Williams-Beuren syndrome | Del(5Gtf2i-Fkbp6)1Vcam/+ | B6.129-Del(5Gtf2i-Fkbp6)1Vcam(J:204278) | J:216195 | View | ||||
Williams-Beuren syndrome | Del(5Gtf2i-Limk1)1Uta/Del(5Limk1-Trim50)2Uta | involves: 129S7/SvEvBrd * C57BL/6J | J:182796 | View | ||||
Williams-Beuren syndrome | Eif4hGt(Ex279)Byg/Eif4hGt(Ex279)Byg | involves: 129P2/OlaHsd * C57BL/6 | J:181945 | View | ||||
Xia-Gibbs Syndrome | Ahdc1em#Oro/? | mosaic involves: C57BL/6 * CD-1 | J:326009 | View | ||||
![]() | abdominal obesity-metabolic syndrome | Ctf1tm1Msd/Ctf1tm1Msd | B6.Cg-Ctf1tm1Msd | J:176727 | View | |||
abdominal obesity-metabolic syndrome | Gucy2ctm1Gar/Gucy2ctm1Gar | B6.129S6-Gucy2ctm1Gar | J:178241 | View | ||||
abdominal obesity-metabolic syndrome | Lepob/Lepob | involves: STOCK Mlphln a Tgfawa1 Cdh23v Ednrbs | J:219470 | View | ||||
abdominal obesity-metabolic syndrome | Neil1tm1Rsld/Neil1tm1Rsld | involves: 129S1/Sv * C57BL/6 | J:106077 | View | ||||
abdominal obesity-metabolic syndrome | Ppargtm1Lja/Pparg+ | involves: 129S1/Sv * 129X1/SvJ | J:98786 | View | ||||
abdominal obesity-metabolic syndrome |
Prkcitm1Rfar/Prkci+ Tg(Ckmm-cre)5Khn/? |
involves: 129P2/OlaHsd * C57BL/6 * FVB | J:123964 | View | ||||
abdominal obesity-metabolic syndrome | Sirt3tm1.1Fwa/Sirt3tm1.1Fwa | involves: 129S6/SvEvTac | J:178653 | View | ||||
abdominal obesity-metabolic syndrome |
Slc2a9tm1Khm/Slc2a9tm1Khm Tg(Vil1-cre)997Gum/0 |
involves: 129 * C57BL/6 * C57BL/6J | J:221544 | View | ||||
abdominal obesity-metabolic syndrome 1 |
Apobtm2Sgy/Apobtm2Sgy Apoetm1Unc/Apoetm1Unc Lepob/Lepob |
involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6 | J:133453 | View | ||||
abdominal obesity-metabolic syndrome 1 |
Apobtm2Sgy/Apobtm2Sgy Ldlrtm1Her/Ldlrtm1Her Lepob/Lepob |
involves: 129S7/SvEvBrd * C57BL/6 | J:133453 | View | ||||
abdominal obesity-metabolic syndrome 1 | Lepob/Lepob | involves: C57BL/6J | J:219118 | View | ||||
abdominal obesity-metabolic syndrome 1 | Trp53inp1tm1Acar/Trp53inp1tm1Acar | involves: 129/Sv * C57BL/6 | J:233434 | View | ||||
age related macular degeneration | Ccl2tm1Rol/Ccl2tm1Rol | B6.129S4-Ccl2tm1Rol | J:147328 | View | ||||
age related macular degeneration |
Ccl2tm1Rol/Ccl2tm1Rol Cx3cr1tm1Litt/Cx3cr1tm1Litt |
involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6J | J:200877 | View | ||||
age related macular degeneration |
Ccl2tm1Rol/Ccl2tm1Rol Cx3cr1tm1Zm/Cx3cr1tm1Zm |
involves: 129 * 129S4/SvJae | J:126935 | View | ||||
age related macular degeneration | Ccr2tm1Mae/Ccr2tm1Mae | B6.129P2-Ccr2tm1Mae | J:147328 | View | ||||
age related macular degeneration | Cd46tm1Atk/Cd46tm1Atk | B6.129-Cd46tm1Atk | J:234294 | View | ||||
age related macular degeneration | Ppargc1atm1Brsp/Ppargc1a+ | involves: 129S4/SvJae * C57BL/6 | J:264271 | View | ||||
age related macular degeneration 1 |
Cryba1tm1.1Dbsa/Cryba1tm1.1Dbsa Tg(BEST1-cre)1Jdun/0 |
involves: 129S6/SvEvTac * C57BL/6 | J:215531 | View | ||||
age related macular degeneration 1 | Vldlrtm1Her/Vldlrtm1Her | B6;129S7-Vldlrtm1Her/J | J:132497 | View | ||||
amyotrophic lateral sclerosis type 1 | Sod2tm1Cje/Sod2tm1Cje | involves: C57BL/6J | J:45913 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(Thy1-Sncg)HvP36Putt/? | C57BL/6-Tg(Thy1-Sncg)HvP36Putt | J:185793 | View | ||||
amyotrophic lateral sclerosis type 1 | Vegfatm2Pec/Vegfatm2Pec | involves: 129S1/Sv * 129X1/SvJ | J:69797 | View | ||||
amyotrophic lateral sclerosis type 1 | Vps54wr/Vps54wr | involves: C57BL/6J * C57BL/Fa | J:181019, J:196432 | View | ||||
arrhythmogenic right ventricular dysplasia 5 | Rpsatp1/Rpsatp1 | involves: KK | J:87868 | View | ||||
autosomal dominant disease | Fgfr3tm1.1Iwa/Fgfr3+ | involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss | J:70061 | View | ||||
autosomal dominant intellectual developmental disorder |
Auts2tm1.1Dare/Auts2tm1.1Dare Tg(Nes-cre)1Kln/0 |
involves: C57BL/6 * SJL | J:217675 | View | ||||
autosomal dominant intellectual developmental disorder | Mbd5Gt(Ayu21-B205)Imeg/Mbd5+ | B6.Cg-Mbd5Gt(Ayu21-B205)Imeg | J:212073 | View | ||||
autosomal dominant intellectual developmental disorder |
Zbtb18tm1.1Nda/Zbtb18tm1.1Nda Tg(Nes-cre)1Kln/0 |
involves: C57BL/6 * SJL | J:184434 | View | ||||
autosomal dominant nonsyndromic deafness 4A | Ceacam16tm1Wzm/Ceacam16tm1Wzm | BALB/cJ-Ceacam16tm1Wzm | J:187537 | View | ||||
autosomal dominant nonsyndromic deafness 25 | Trpv4tm1Msz/Trpv4tm1Msz | involves: 129X1/SvJ * C57BL/6 | J:104851 | View | ||||
autosomal dominant polycystic kidney disease | Bicc1jcpk/Bicc1+ | involves: 101 * C3H * T STOCK | J:23047 | View | ||||
autosomal dominant polycystic kidney disease | Nphp3pcy/Nphp3pcy | either: D2.KK-Nphp3pcy or (involves: DBA/2Fg * DBA/2J * KK) | J:11399 | View | ||||
autosomal dominant polycystic kidney disease | Nphp3pcy/Nphp3pcy | involves: KK | J:244067 | View | ||||
autosomal dominant polycystic kidney disease | Nphp3pcy/Nphp3pcy | KK-Nphp3pcy | J:8302 | View | ||||
autosomal dominant polycystic kidney disease | Tg(HBB-Myc)#Cos/0 | involves: C57BL/6J * CBA/J | J:45203 | View | ||||
Axenfeld-Rieger syndrome type 1 | Tg(KRT14-Hmgn2)#Baam/0 | Not Specified | J:203117 | View | ||||
Axenfeld-Rieger syndrome type 3 | Bmp4tm1Blh/Bmp4+ | B6.129S2-Bmp4tm1Blh | J:82877 | View | ||||
cataract 2 multiple types | CrygdLop12/Crygd+ | involves: BALB/cJ * SJL/J | J:60856 | View | ||||
central conducting lymphatic anomaly | Mdficem1Nlh/Mdficem2Nlh | C57BL/6J-Mdficem1Nlh/Mdficem2Nlh | J:326462 | View | ||||
cleidocranial dysplasia | Ccd/Ccd+ | B10Rl.101-Ccd | J:16170 | View | ||||
cleidocranial dysplasia | Ccd/Ccd+ | involves: 101 * C3H | J:14006 | View | ||||
Coffin-Siris syndrome |
Arid1atm1.1Mag/Arid1a+ H2az2Tg(Wnt1-cre)11Rth/H2az2+ |
involves: C57BL/6J * CBA/J | J:231470 | View | ||||
Coffin-Siris syndrome |
Arid1atm1.1Mag/Arid1atm1.1Mag H2az2Tg(Wnt1-cre)11Rth/H2az2+ |
involves: C57BL/6J * CBA/J | J:231470 | View | ||||
congenital central hypoventilation syndrome | Tlx3tm1Sjk/Tlx3tm1Sjk | involves: 129X1/SvJ | J:60751 | View | ||||
DiGeorge syndrome | Aldh1a2tm1Dll/Aldh1a2tm1Ipc | involves: CD-1 | J:81969 | View | ||||
DiGeorge syndrome | b2b954Clo/b2b954Clo | C57BL/6J-b2b954Clo | J:175213 | View | ||||
DiGeorge syndrome | b2b1941Clo/b2b1941Clo | C57BL/6J-b2b1941Clo | J:175213 | View | ||||
DiGeorge syndrome | b2b2696Clo/b2b2696Clo | C57BL/6J-b2b2696Clo | J:175213 | View | ||||
DiGeorge syndrome | Chrdtm1Emdr/Chrdtm1Emdr | either: B6SJL.129-Chrdtm1Emdr or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SJL/J) | J:83662 | View | ||||
DiGeorge syndrome | Crkltm1Imo/Crkltm1Imo | involves: 129S4/SvJaeSor * C57BL/6J | J:67826 | View | ||||
DiGeorge syndrome |
Dicer1tm1Bdh/Dicer1tm1Bdh H2az2Tg(Wnt1-cre)11Rth/H2az2+ |
involves: 129 * C57BL/6 * CBA/J | J:166758 | View | ||||
DiGeorge syndrome | Dock1b2b3190Clo/Dock1b2b3190Clo | C57BL/6J-Dock1b2b3190Clo | J:175213 | View | ||||
DiGeorge syndrome |
Fgf8tm1.3Mrt/Fgf8tm1.4Mrt Tg(Tbx1-cre)1Joe/0 |
involves: 129P2/OlaHsd | J:88814 | View | ||||
DiGeorge syndrome | Foxn1nu/Foxn1nu | Not Specified | J:202300 | View | ||||
DiGeorge syndrome | Hoxa3tm1Mrc/Hoxa3tm1Mrc | involves: 129S7/SvEvBrd | J:17753 | View | ||||
DiGeorge syndrome | Kat6atm1Avo/Kat6atm1Avo | involves: 129/Sv * BALB/c * FVB/N | J:188772 | View | ||||
DiGeorge syndrome | Ndst1b2b2230Clo/Ndst1b2b2230Clo | C57BL/6J-Ndst1b2b2230Clo | J:175213 | View | ||||
DiGeorge syndrome | Plxnd1b2b1863Clo/Plxnd1b2b1863Clo | C57BL/6J-Plxnd1b2b1863Clo | J:175213 | View | ||||
DiGeorge syndrome | Plxnd1b2b3150Clo/Plxnd1b2b3150Clo | C57BL/6J-Plxnd1b2b3150Clo | J:175213 | View | ||||
DiGeorge syndrome | pta/pta | C57BL/6J-pta | J:94456 | View | ||||
DiGeorge syndrome |
Tgfbr2tm1Karl/Tgfbr2tm1Karl H2az2Tg(Wnt1-cre)11Rth/H2az2+ |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA | J:96359 | View | ||||
DiGeorge syndrome | Vegfatm1Pec/Vegfatm1Pec | involves: 129S1/Sv * 129X1/SvJ | J:81698 | View | ||||
DiGeorge syndrome | Vegfatm4Pec/Vegfatm4Pec | involves: 129S1/Sv * 129X1/SvJ | J:81698 | View | ||||
DiGeorge syndrome | Zfp366b2b2834Clo/Zfp366b2b2834Clo | C57BL/6J-Zfp366b2b2834Clo | J:175213 | View | ||||
dilated cardiomyopathy 1A |
Dot1ltm1Tche/Dot1ltm1.1Tche Tg(Myhca-cre)1Abel/0 |
Not Specified | J:168140 | View | ||||
Ehlers-Danlos syndrome classic type 1 | Col5a2tm1.2Dgr/Col5a2+ | involves: 129S7/SvEvBrd * C57BL/6 * DBA/2 | J:223298 | View | ||||
Ehlers-Danlos syndrome classic type 1 |
Fmodtm1Aol/Fmodtm1Aol Lumtm1Chak/Lumtm1Chak |
involves: 129S1/Sv * 129X1/SvJ * CD-1 | J:79115 | View | ||||
Ehlers-Danlos syndrome classic type 1 | Lumtm1Chak/Lumtm1Chak | involves: 129S/Sv * CD-1 | J:48068 | View | ||||
epidermolysis bullosa simplex Dowling-Meara type | Krt5tm1Tmm/Krt5tm1Tmm | involves: 129P2/OlaHsd * BALB/c | J:76311 | View | ||||
epidermolysis bullosa simplex Dowling-Meara type |
Krt14tm1Der/Krt14+ Tg(KRT5-cre/PGR)1Der/? |
involves: 129X1/SvJ * FVB * ICR | J:67320 | View | ||||
epidermolysis bullosa simplex Dowling-Meara type |
Krt14tm1Der/Krt14+ Tg(KRT14-cre/PGR)1Der/? |
involves: 129X1/SvJ * FVB * ICR | J:67320 | View | ||||
epidermolysis bullosa simplex Dowling-Meara type | Krt14tm2Der/Krt14+ | involves: 129X1/SvJ | J:67320 | View | ||||
familial medullary thyroid carcinoma | Prlrtm1Cnp/Prlrtm1Cnp | involves: 129/Sv * 129P2/OlaHsd | J:101609 | View | ||||
fibrodysplasia ossificans progressiva | Tg(Eno2-Bmp4)3Jake/0 | involves: BALB/c * C57BL/6 | J:93682 | View | ||||
Grn-related frontotemporal lobar degeneration with Tdp43 inclusions | Tg(Camk2a-Tardbp)#Ckjs/Tg(Camk2a-Tardbp)#Ckjs | FVB/N-Tg(Camk2a-Tardbp)#Ckjs | J:163612 | View | ||||
hereditary multiple exostoses | Ext2tm1Werb/Ext2+ | involves: C57BL/6 | J:103125 | View | ||||
hereditary spherocytosis type 1 | Add2tm1Llp/Add2tm1Llp | involves: 129S4/SvJae * C57BL/6J | J:71029 | View | ||||
hereditary spherocytosis type 1 | Epb42tm1Llp/Epb42tm1Llp | involves: 129P2/OlaHsd * C57BL/6J | J:67412 | View | ||||
hereditary spherocytosis type 1 | Spta1sph-2Bc/Spta1sph-2Bc | involves: SELH | J:7048, J:7501 | View | ||||
hereditary spherocytosis type 1 | Spta1sph-ha/Spta1sph-ha | involves: DBA/1J | J:14946, J:30699 | View | ||||
hereditary spherocytosis type 1 | Spta1sph/Spta1sph | involves: C3H | J:12276 | View | ||||
hereditary spherocytosis type 4 | Slc4a1wan/Slc4a1wan | C3H/HeJ-Slc4a1wan/J | J:89043 | View | ||||
Holt-Oram syndrome | vsd/vsd | C57BL/6J-vsd | J:94456 | View | ||||
Holt-Oram syndrome | vsd/vsd+ | C57BL/6J-vsd | J:94456 | View | ||||
hypotrichosis 4 | HrHp/HrHp | BALB/cJ-HrHp | J:150720 | View | ||||
ichthyosis vulgaris | Lbric-J/Lbric-J | involves: 129S4/SvJae * C57BL/6 | J:143838 | View | ||||
idiopathic pulmonary fibrosis | Tg(H2-K-Fosl2,-EGFP)13Wag/0 | either: 129.Cg-Tg(H2-K-Fosl2,-EGFP)13Wag or B6.Cg-Tg(H2-K-Fosl2,-EGFP)13Wag | J:139032 | View | ||||
idiopathic pulmonary fibrosis | Tg(SFTPC-Tnf)2Pva/0 | involves: C57BL/6 * DBA/2 | J:28120 | View | ||||
juvenile glaucoma |
Pax6tm2Pgr/Pax6+ Tg(Pax6-cre,GFP)1Pgr/0 |
involves: 129S1/Sv * 129X1/SvJ * FVB | J:163191 | View | ||||
lacrimoauriculodentodigital syndrome 1 | Fgf10tm1Wss/Fgf10+ | involves: 129X1/SvJ | J:237227 | View | ||||
Loeys-Dietz syndrome |
Fbn1tm1Hcd/Fbn1+ Tgfb2tm1Doe/Tgfb2+ |
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6J | J:188799 | View | ||||
Loeys-Dietz syndrome | Tgfb2tm1Doe/Tgfb2+ | STOCK Tgfb2tm1Doe/J | J:188799 | View | ||||
Loeys-Dietz syndrome | Tgfbr1tm1.1Hcd/Tgfbr1+ | 129S6(Cg)-Tgfbr1tm1.1Hcd | J:204960 | View | ||||
Loeys-Dietz syndrome | Tgfbr2tm1.1Hcd/Tgfbr2+ | 129S6(Cg)-Tgfbr2tm1.1Hcd | J:204960 | View | ||||
maturity-onset diabetes of the young |
Ins1tm1Jja/Ins1tm1Jja Ins2tm1Jja/Ins2tm1Jja |
involves: 129S2/SvPas | J:40377, J:77595 | View | ||||
maturity-onset diabetes of the young | Ins2Akita/Ins2+ | C57BL/6-Ins2Akita | J:40063 | View | ||||
maturity-onset diabetes of the young | Ins2Akita/Ins2+ | C57BL/6-Ins2Akita/J | J:99412 | View | ||||
maturity-onset diabetes of the young | Mafatm1Staka/Mafatm1Staka | involves: ICR | J:99126 | View | ||||
maturity-onset diabetes of the young | Pdx1tm1Ted/Pdx1+ | involves: 129P2/OlaHsd | J:48516, J:82969 | View | ||||
maturity-onset diabetes of the young | Tgm2tm1Gml/Tgm2tm1Gml | involves: 129X1/SvJ * C57BL/6 | J:75566, J:78633, J:82489 | View | ||||
Miller-Dieker lissencephaly syndrome |
Dph1tm1.1Cmch/Dph1tm1.1Cmch Edil3Tg(Sox2-cre)1Amc/Edil3+ |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6J * CBA | J:214744 | View | ||||
Miller-Dieker lissencephaly syndrome |
Dph1tm1.1Cmch/Dph1tm1.1Cmch H2az2Tg(Wnt1-cre)11Rth/H2az2+ |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J | J:214744 | View | ||||
Miller-Dieker lissencephaly syndrome | Dph1tm2Bhr/Dph1tm2Bhr | involves: 129S4/SvJae * C57BL/6J | J:214744 | View | ||||
Miller-Dieker lissencephaly syndrome | Hic1tm1Sbb/Hic1tm1Sbb | involves: 129S4/SvJae * C57BL/6 | J:60589 | View | ||||
Miller-Dieker lissencephaly syndrome | Mnttm1.1Awb/Mnttm1.1Awb | involves: 129S6/SvEvTac * FVB/N | J:90397 | View | ||||
Miller-Dieker lissencephaly syndrome | Pafah1b1tm1Awb/Pafah1b1+ | involves: 129S6/SvEvTac * NIH Black Swiss | J:49531, J:59817 | View | ||||
Miller-Dieker lissencephaly syndrome |
Pafah1b1tm1Awb/Pafah1b1+ Ywhaetm1Awb/Ywhae+ |
either: 129S6/SvEvTac or (involves: 129S6/SvEvTac * NIH Black Swiss) | J:84075 | View | ||||
Miller-Dieker lissencephaly syndrome | Pafah1b1tm1Awb/Pafah1b1tm2Awb | involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss | J:49531 | View | ||||
Miller-Dieker lissencephaly syndrome | Pafah1b1tm1Or/Pafah1b1+ | Not Specified | J:69631 | View | ||||
Miller-Dieker lissencephaly syndrome | Pafah1b1tm2.2Awb/Pafah1b1+ | involves: 129S6/SvEvTac * NIH Black Swiss | J:49531 | View | ||||
Miller-Dieker lissencephaly syndrome | Ywhaetm1Awb/Ywhaetm1Awb | either: 129S6/SvEvTac or (involves: 129S6/SvEvTac * NIH Black Swiss) | J:84075 | View | ||||
Muir-Torre syndrome | Fhittm1Hbn/Fhit+ | involves: 129X1/SvJ * C57BL/6 | J:61946 | View | ||||
multiple synostoses syndrome | Fgf9tm1Zgwg/Fgf9+ | involves: 129S1/Sv | J:241783 | View | ||||
multiple synostoses syndrome | Fgf9tm1Zgwg/Fgf9tm1Zgwg | involves: 129S1/Sv | J:241783 | View | ||||
multiple synostoses syndrome | Gdf5Bp-5J/Gdf5+ | C57BL/6J-Gdf5Bp-5J/GrsrJ | J:200816 | View | ||||
myofibrillar myopathy 1 | Ldb3tm1Chen/Ldb3tm1Chen | involves: 129S1/Sv * 129X1/SvJ * Black Swiss | J:72799 | View | ||||
nail-patella syndrome |
Ldb1tm1Witz/Ldb1tm1Witz Tg(NPHS2-cre)295Lbh/0 |
involves: C57BL/6 * SJL | J:122505 | View | ||||
Noonan syndrome with multiple lentigines | Ptpn11tm1.1Ics/Ptpn11+ | involves: 129S2/SvPas * C57BL/6 * FVB/N | J:216593 | View | ||||
Noonan syndrome with multiple lentigines | Ptpn11tm4.2Bgn/Ptpn11+ | involves: 129S6/SvEvTac * C57BL/6J * FVB/N | J:172033 | View | ||||
Noonan syndrome with multiple lentigines | Tg(Myh7-Ptpn11*Q510E)#Krnz/0 | FVB/N-Tg(Myh7-Ptpn11*Q510E)#Krnz | J:222124 | View | ||||
ocular albinism with sensorineural deafness | MitfMi-Crc/Mitf+ | involves: CBA/CaCrc | J:83500 | View | ||||
ocular albinism with sensorineural deafness | MitfMi-Crc/MitfMi-Crc | involves: CBA/CaCrc | J:83500 | View | ||||
ocular albinism with sensorineural deafness | Mitfmi-enu122/Mitf+ | involves: 102 * C3H | J:46254 | View | ||||
ocular albinism with sensorineural deafness | Mitfmi-enu122/Mitfmi-enu122 | involves: 102 * C3H | J:46254 | View | ||||
ocular albinism with sensorineural deafness | MitfMi-H/Mitf+ | involves: BALB/cAnN * C3H/HeN | J:75964 | View | ||||
ocular albinism with sensorineural deafness | MitfMi-H/MitfMi-H | involves: BALB/cAnN * C3H/HeN | J:75964 | View | ||||
ocular albinism with sensorineural deafness | MitfMi-H/MitfRorp | involves: BALB/cAnN * C3H/HeN | J:75964 | View | ||||
ocular albinism with sensorineural deafness | MitfMi-wh/Mitf+ | involves: C57BL * DBA | J:13058 | View | ||||
ocular albinism with sensorineural deafness | MitfMi-wh/MitfMi-wh | involves: C57BL * DBA | J:13058 | View | ||||
ocular albinism with sensorineural deafness | MitfMi-wh/Mitfmi-x | involves: NZB/Mac | J:83501 | View | ||||
ocular albinism with sensorineural deafness | Mitfmi-x/Mitfmi-x | involves: NZB/Mac | J:83501 | View | ||||
ocular albinism with sensorineural deafness | MitfMi/MitfMi | Not Specified | J:30758 | View | ||||
ocular albinism with sensorineural deafness | MitfRorp/Mitf+ | involves: BALB/cAnN * C3H/HeN | J:75964 | View | ||||
ocular albinism with sensorineural deafness | MitfRorp/MitfRorp | involves: BALB/cAnN * C3H/HeN | J:75964 | View | ||||
osteogenesis imperfecta type 2 | Smpd3fro/Smpd3fro | Not Specified | J:3906 | View | ||||
osteogenesis imperfecta type 3 | Smpd3fro/Smpd3fro | Not Specified | J:3906 | View | ||||
osteogenesis imperfecta type 5 | SucoGt(KST050)Byg/SucoGt(KST050)Byg | involves: 129P2/OlaHsd * C57BL/6 * CD-1 | J:159823 | View | ||||
PCWH syndrome | Mpztm1Msch/Mpz+ | involves: 129S7/SvEvBrd * C57BL/6 | J:82432 | View | ||||
polycystic liver disease |
Prkcshtm1Som/Prkcshtm1Som Tg(CAG-cre/Esr1*)1Lbe/0 |
involves: 129 * 129S1/Sv * 129X1/SvJ * C57BL/6 | J:188763 | View | ||||
polycystic liver disease | Ucp2tm1Lowl/Ucp2tm1Lowl | B6.129S4-Ucp2tm1Lowl | J:272325 | View | ||||
popliteal pterygium syndrome | Ripk4tm1Pmh/Ripk4tm1Pmh | involves: 129 * C57BL/6 | J:183160, J:191507 | View | ||||
progeria | Sirt6tm1Fwa/Sirt6tm1Fwa | involves: 129S6/SvEvTac * 129X1/SvJ | J:112817 | View | ||||
progeria | Vcpip1em1Zlou/Vcpip1em1Zlou | C57BL/6NHsd-Vcpip1em1Zlou | J:297179 | View | ||||
progeria | Zmpste24tm1Otin/Zmpste24tm1Otin | involves: 129P2/OlaHsd | J:164373 | View | ||||
progeria | Zmpste24tm1Sgy/Zmpste24tm1Sgy | B6.129S4-Zmpste24tm1Sgy | J:106706 | View | ||||
progeria | Zmpste24tm1Sgy/Zmpste24tm1Sgy | involves: 129S4/SvJae * C57BL/6 | J:95274 | View | ||||
spinocerebellar ataxia type 27 | Fgf14tm1Dor/Fgf14tm1Dor | B6.129S6-Fgf14tm1Dor | J:134733 | View | ||||
split hand-foot malformation 1 | Dlx5/Dlx6tm1Levi/Dlx5/Dlx6tm1Levi | Not Specified | J:77244 | View | ||||
spondyloepiphyseal dysplasia congenita | Hapln1tm1Nid/Hapln1tm1Nid | involves: 129S1/Sv * 129X1/SvJ | J:52575 | View | ||||
Stargardt disease | Abca4tm1.1Rsmy/Abca4tm1.1Rsmy | involves: C57BL/6 | J:255529 | View | ||||
Stargardt disease | Abca4tm1Ght/Abca4tm1Ght | involves: 129S4/SvJae | J:141801 | View | ||||
Stargardt disease | Abca4tm1Ght/Abca4tm1Ght | involves: 129S4/SvJae * BALB/c | J:141801 | View | ||||
Stargardt disease | Abca4tm1Ght/Abca4tm1Ght | involves: 129S4/SvJae * C57BL/6 | J:56317 | View | ||||
Stargardt disease |
Abca4tm1Kpal/Abca4tm1Kpal Rdh8tm1Kpal/Rdh8tm1Kpal |
involves: 129 | J:213619 | View | ||||
Stargardt disease | Elovl4tm1Rayy/Elovl4+ | involves: 129 * C57BL/6J | J:114752 | View | ||||
Stargardt disease | Elovl4tm1Wked/Elovl4+ | involves: 129S/SvEv * 129S1/Sv | J:121481 | View | ||||
type 1 diabetes mellitus 2 |
Apobtm2Sgy/Apobtm2Sgy Ldlrtm1Her/Ldlrtm1Her Tg(Ins-Igf2)1Fbos/? |
involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6J * SJL | J:227165 | View | ||||
type 1 diabetes mellitus 2 | Tg(Ins-Igf2)1Fbos/0 | involves: C57BL/6 * C57BLKs/J * SJL | J:141527 | View | ||||
type 1 diabetes mellitus 2 | Tg(Ins-Igf2)1Fbos/0 | involves: C57BL/6 * SJL | J:141527 | View | ||||
Ullrich congenital muscular dystrophy | Col6a1tm1Sngi/Col6a1tm1Sngi | B6.Cg-Col6a1tm1Sngi | J:278926 | View | ||||
Ullrich congenital muscular dystrophy | Col6a3tm2.1Chu/Col6a3+ | B6.129(Cg)-Col6a3tm2.1Chu | J:208903 | View | ||||
Waardenburg syndrome | Aebp2Gt(BC0681)Wtsi/Aebp2+ | involves: 129P2/OlaHsd * C57BL/6 | J:177673 | View | ||||
Waardenburg syndrome | Snai2tm2Grid/Snai2tm2Grid | involves: 129S1/Sv | J:80529 | View | ||||
Waardenburg syndrome type 1 | MitfMi-Crc/Mitf+ | involves: CBA/CaCrc | J:83500 | View | ||||
Williams-Beuren syndrome | b2b370Clo/b2b370Clo | C57BL/6J-b2b370Clo | J:175213 | View | ||||
Williams-Beuren syndrome | Baz1bMommeD10/Baz1b+ | involves: FVB/N | J:142335 | View | ||||
Williams-Beuren syndrome | Baz1bMommeD10/Baz1bMommeD10 | involves: FVB/N | J:142335 | View | ||||
Williams-Beuren syndrome | Baz1btm1Ska/Baz1b+ | involves: C57BL/6 * CBA | J:149990 | View | ||||
Williams-Beuren syndrome | Baz1btm1Ska/Baz1btm1Ska | involves: C57BL/6 * CBA | J:149990 | View | ||||
Williams-Beuren syndrome | Clip2tm1.1Gal/Clip2+ | involves: 129P2/OlaHsd * C57BL/6 | J:78711 | View | ||||
Williams-Beuren syndrome | Dlg4tm2.1Grnt/Dlg4tm2.1Grnt | involves: 129P2/OlaHsd * C57BL/6J | J:175436 | View | ||||
Williams-Beuren syndrome | Fzd9tm1Sjp/Fzd9tm1Sjp | involves: C57BL/6J | J:99893 | View | ||||
Williams-Beuren syndrome | Fzd9tm1Uta/Fzd9+ | involves: 129X1/SvJ | J:169924 | View | ||||
Williams-Beuren syndrome | Gtf2iGt(XE029)Byg/Gtf2i+ | involves: 129P2/OlaHsd * C57BL/6 | J:143508 | View | ||||
Williams-Beuren syndrome | Gtf2itm1Vcam/Gtf2itm1Vcam | involves: 129S1/Sv * 129X1/SvJ * CD-1 | J:204278 | View | ||||
Williams-Beuren syndrome | Gtf2ird1Gt(XE465)Byg/Gtf2ird1+ | involves: 129P2/OlaHsd * C57BL/6 | J:143508 | View | ||||
Williams-Beuren syndrome | Gtf2ird1Tg(Alb1-Myc)166.8Sst/Gtf2ird1Tg(Alb1-Myc)166.8Sst | involves: C57BL/6 * CBA | J:102709 | View | ||||
Williams-Beuren syndrome | Gtf2ird1Tg(Alb1-Myc)166.8Sst/Gtf2ird1Tg(Alb1-Myc)166.8Sst | involves: C57BL/6J * CBA/J | J:190478 | View | ||||
Williams-Beuren syndrome | Gtf2ird1tm1Hrd/Gtf2ird1tm1Hrd | involves: 129S1/Sv * 129X1/SvJ * C57BL/6J | J:182346 | View | ||||
Williams-Beuren syndrome | Limk1tm1Zpj/Limk1tm1Zpj | involves: 129 | J:86283 | View | ||||
Williams-Beuren syndrome | Loxb2b370.2Clo/Loxb2b370.2Clo | C57BL/6J-Loxb2b370.2Clo | J:175213 | View | ||||
Williams-Beuren syndrome | Srcinl/Srcinl | involves: 129 | J:229610 | View | ||||
![]() | age related macular degeneration 1 | Apoetm3(APOE*4)Mae/Apoetm3(APOE*4)Mae | involves: 129P2/OlaHsd * C57BL/6 | J:101147 | View | |||
age related macular degeneration 2 |
Abca4tm1Ght/Abca4tm1Ght Rdh8tm1Kpal/Rdh8tm1Kpal |
involves: 129 * 129S4/SvJae | J:154536 | View | ||||
Alzheimer's disease 4 |
Psen1tm1Jzt/Psen1tm1Jzt Psen2tm1Ber/Psen2tm1Ber Tg(Camk2a-cre)T29-1Stl/0 |
involves: C57BL/6 * CBA | J:90685 | View | ||||
dilated cardiomyopathy 1E | Scn5atm1(SCN5A)Rdn/Scn5atm3(SCN5A*)Rdn | involves: 129S6/SvEvTac | J:189389 | View | ||||
dilated cardiomyopathy 1E | Scn5atm3(SCN5A*)Rdn/Scn5atm3(SCN5A*)Rdn | involves: 129S6/SvEvTac | J:189389 | View | ||||
familial erythrocytosis 1 | Eportm1.4Jtp/Epor+ | involves: 129P2/OlaHsd * C57BL/6 | J:67205 | View | ||||
familial erythrocytosis 1 | Eportm1.4Jtp/Eportm1.4Jtp | involves: 129P2/OlaHsd * C57BL/6 | J:67205 | View | ||||
hereditary breast ovarian cancer syndrome |
Brca1tm1Cxd/Brca1tm2Cxd Trp53tm1Brd/Trp53+ Tg(MMTV-cre)4Mam/0 |
involves: 129S6/SvEvTac * 129S7/SvEvBrd * Black Swiss * FVB | J:54533 | View | ||||
hereditary breast ovarian cancer syndrome |
Brca1tm2Cxd/Brca1tm2Cxd Tg(MMTV-cre)4Mam/0 Tg(MMTV-rtTA)1Lach/0 Tg(tetO-Esr1)#Paf/0 Trp53tm1Brd/Trp53+ |
involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6 * FVB | J:132088 | View | ||||
hereditary breast ovarian cancer syndrome |
Brca1tm2Cxd/Brca1tm2Cxd Trp53tm1Brd/Trp53+ Tg(MMTV-cre)4Mam/0 |
involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6 * FVB | J:132088 | View | ||||
Machado-Joseph disease | Atxn3tm2.1(ATXN3*)Mfig/Atxn3+ | involves: 129 * C57BL/6J | J:218541 | View | ||||
pachyonychia congenita |
Krt17tm1Cou/Krt17tm1Cou Krt6a/Krt6btm1Cou/Krt6a/Krt6btm1Cou Krt6a/Krt6btm1Cou/Krt6a/Krt6btm1Cou |
involves: 129S2/SvPas * C57BL/6 | J:95390 | View | ||||
spinocerebellar ataxia type 15 |
Glatm1Kul/Glatm1Kul Itpr1wblo/Itpr1wblo |
B6;129-Glatm1Kul Itpr1wblo/GrsrJ | J:222308 | View | ||||
spinocerebellar ataxia type 15 |
Glatm1Kul/Y Itpr1wblo/Itpr1wblo |
B6;129-Glatm1Kul Itpr1wblo/GrsrJ | J:222308 | View | ||||
Transgenes and Other Mutations | abdominal obesity-metabolic syndrome | Tg(RP11-578M14)5Mkru/0 | involves: FVB/N | J:256501 | View | |||
abdominal obesity-metabolic syndrome 1 | Tg(Fabp4-ENPP1)#Naba/0 | involves: C57BL/6J | J:182179 | View | ||||
abdominal obesity-metabolic syndrome 1 | Tg(Fabp4-Hsd11b1)7Jesf/0 | FVB-Tg(Fabp4-Hsd11b1)7Jesf | J:107046 | View | ||||
adult-onset autosomal dominant demyelinating leukodystrophy | Tg(Plp1-LMNB1)1108Qsp/0 | involves: FVB/N | J:226169 | View | ||||
adult-onset autosomal dominant demyelinating leukodystrophy | Tg(Plp1-Lmnb1)#Yfu/0 | involves: FVB | J:197168 | View | ||||
advanced sleep phase syndrome 1 | Tg(PER2*S662G)867Ljp/0 | involves: C57BL/6 | J:126404 | View | ||||
advanced sleep phase syndrome 2 | Tg(CSNK1D*,-EGFP)816Yfu/? | involves: C57BL/6 * SJL | J:97658 | View | ||||
advanced sleep phase syndrome 2 | Tg(CSNK1D*,-EGFP)827Yfu/? | involves: C57BL/6 * SJL | J:97658 | View | ||||
age related macular degeneration 1 | Tg(APOB)1102Sgy/? | B6.Cg-Tg(APOB)1102Sgy | J:151253 | View | ||||
Alexander disease | Tg(GFAP)7Mes/0 | involves: FVB/N | J:99256 | View | ||||
Alexander disease | Tg(GFAP)10Mes/0 | involves: FVB/N | J:99256 | View | ||||
Alexander disease | Tg(Gfap-GFAP*R239H)60TMIke/0 | involves: C57BL/6J | J:139349, J:138318 | View | ||||
Alzheimer's disease 3 |
Tg(APP695)3Dbo/0 Tg(PSEN1dE9)S9Dbo/0 |
B6.Cg-Tg(APP695)3Dbo Tg(PSEN1dE9)S9Dbo/Mmjax | J:157228 | View | ||||
Alzheimer's disease 3 |
Tg(APP695)3Dbo/0 Tg(PSEN1dE9)S9Dbo/0 |
involves: 129S1/Sv * 129X1/SvJ * C3H/HeJ * C57BL/6J | J:123534 | View | ||||
Alzheimer's disease 3 |
Tg(APP695)3Dbo/0 Tg(PSEN1dE9)S9Dbo/0 |
involves: C3H/HeJ * C57BL/6J | J:123534 | View | ||||
Alzheimer's disease 3 | Tg(APPswe,PSEN1dE9)85Dbo/0 | B6;C3-Tg(APPswe,PSEN1dE9)85Dbo/Mmjax | J:113199 | View | ||||
Alzheimer's disease 3 | Tg(APPswe,PSEN1dE9)85Dbo/0 | involves: C3H/HeJ * C57BL/6J | J:87691, J:113200 | View | ||||
Alzheimer's disease 3 | Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas/0 | involves: C57BL/6 * SJL | J:112949 | View | ||||
Alzheimer's disease 3 | Tg(PSEN1dE9)S9Dbo/0 | involves: C3H/HeJ * C57BL/6J | J:104147 | View | ||||
Alzheimer's disease 3 | Tg(PSEN1H163R)G9Btla/0 | involves: 129S4/SvJae | J:58050 | View | ||||
Alzheimer's disease 4 | Tg(APP695)3Dbo/0 | B6.C3-Tg(APP695)3Dbo | J:109847 | View | ||||
Alzheimer's disease 4 |
Tg(APP695)3Dbo/0 Tg(PSEN1)5Dbo/0 |
involves: C3H/HeJ * C57BL/6J | J:43788 | View | ||||
Alzheimer's disease 4 |
Tg(APP695)3Dbo/0 Tg(PSEN1dE9)S9Dbo/0 |
involves: C3H/HeJ * C57BL/6J | J:123534 | View | ||||
amyotrophic lateral sclerosis type 1 |
Cybbtm1Din/Y Tg(SOD1*G93A)dl1Gur/0 |
B6.Cg-Cybbtm1Din Tg(SOD1*G93A)dl1Gur | J:111782 | View | ||||
amyotrophic lateral sclerosis type 1 |
Isl1tm1(cre)Tmj/Isl1+ Tg(SOD1*G37R)1Dwc/0 |
involves: 129X1/SvJ * C57BL/6 | J:109131 | View | ||||
amyotrophic lateral sclerosis type 1 |
Tg(ITGAM-cre)2781Gkl/0 Tg(SOD1*G37R)1Dwc/0 |
involves: C57BL/6 * CBA | J:109131 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(Myl1-SOD1*G93A)#Amu/0 | FVB/NJ-Tg(Myl1-SOD1*G93A)#Amu | J:143747 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(NEFH)200Jpj/0 | Not Specified | J:69180 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(NEFH)200Jpj/Tg(NEFH)200Jpj | Not Specified | J:69180 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(NFH)120Jpj/0 | Not Specified | J:69180 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(NFH)120Jpj/Tg(NFH)120Jpj | Not Specified | J:69180 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(Prnp-Immt/SOD1*G93A)7Gmnf/Tg(Prnp-Immt/SOD1*G93A)7Gmnf | involves: C57BL/6 * CBA * SJL | J:177846 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(Prnp-SOD1*G37R,-PSEN1)110Dbo/Tg(Prnp-SOD1*G37R,-PSEN1)110Dbo | involves: C3H * C57BL/6 | J:104655 | View | ||||
amyotrophic lateral sclerosis type 1 |
Tg(SOD1)2Gur/0 Tg(SOD1*)D-14Dbo/0 |
involves: C3H/HeJ * C57BL/6 * C57BL/6J * SJL | J:218091 | View | ||||
amyotrophic lateral sclerosis type 1 |
Tg(SOD1)2Gur/0 Tg(SOD1*G85R)#Roos/0 |
involves: C57BL/6 * C57BL/6J * SJL | J:147156 | View | ||||
amyotrophic lateral sclerosis type 1 |
Tg(SOD1)2Gur/0 Tg(SOD1*G93A)1Gur/0 |
involves: C57BL/6 * SJL | J:109458 | View | ||||
amyotrophic lateral sclerosis type 1 |
Tg(SOD1)2Gur/0 Tg(SOD1*L126Z)#Deng/0 |
involves: C57BL/6 * SJL | J:109458 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(SOD1*)125Dbo/? | involves: C3H/HeJ * C57BL/6J | J:86421 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(SOD1*)D-14Dbo/0 | involves: C3H/HeJ * C57BL/6J | J:218091 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(SOD1*)DF7Yaw/0 | C57BL/6-Tg(SOD1*)DF7Yaw | J:97932 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(SOD1*)DF7Yaw/Tg(SOD1*)DF7Yaw | C57BL/6-Tg(SOD1*)DF7Yaw | J:97932 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(SOD1*G37R)9Dpr/0 | involves: C3H/HeJ * C57BL/6J | J:69178 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(SOD1*G37R)29Dpr/0 | involves: C3H/HeJ * C57BL/6J | J:69178, J:119631 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(SOD1*G37R)42Dpr/0 | involves: C3H/HeJ * C57BL/6J | J:69178 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(SOD1*G37R)106Dpr/0 | involves: C3H/HeJ * C57BL/6J | J:69178 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(SOD1*G85R)74Dwc/? | Not Specified | J:77600 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(SOD1*G85R)148Dwc/? | Not Specified | J:77600 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(SOD1*G85R)#Roos/0 | involves: C57BL/6J | J:147156 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(SOD1*G85R/EYFP)641Alho/Tg(SOD1*G85R/EYFP)641Alho | involves: C57BL/6J * SJL/J | J:144475 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(SOD1*G85R/EYFP)737Alho/Tg(SOD1*G85R/EYFP)737Alho | involves: C57BL/6J * SJL/J | J:212250 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(SOD1*G93A)1Gur/0 | B6.Cg-Tg(SOD1*G93A)1Gur | J:155140 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(SOD1*G93A)1Gur/0 | B6.Cg-Tg(SOD1*G93A)1Gur/J | J:211734 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(SOD1*G93A)1Gur/0 | B6SJL-Tg(SOD1*G93A)1Gur | J:144199 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(SOD1*G93A)1Gur/0 | B6SJL-Tg(SOD1*G93A)1Gur/J | J:133155, J:143173, J:146652, J:212250 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(SOD1*G93A)1Gur/0 | involves: C57BL/6 * SJL | J:76718, J:91800, J:109458, J:130581 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(SOD1*G93A)2Gur/0 | involves: C57BL/6 * SJL | J:32665, J:78629, J:89928 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(SOD1*G93A)dl1Gur/0 | involves: C57BL/6 * SJL | J:106420 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(SOD1*G127X)716Mrkl/Tg(SOD1*G127X)716Mrkl | B6JBom.Cg-Tg(SOD1*G127X)716Mrkl | J:175594 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(SOD1*H46R)#Maw/0 | involves: C57BL/6 * DBA/2 | J:99701 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(SOD1*H46R)IAra/0 | involves: C57BL/6 * DBA/2 | J:221350 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(SOD1*H46R)LAra/0 | involves: C57BL/6 * DBA/2 | J:221350 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(SOD1*H46R*H48Q)58Dbo/0 | involves: C3H/HeJ * C57BL/6J | J:119631 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(SOD1*H46R*H48Q)139Dbo/0 | involves: C3H/HeJ * C57BL/6J | J:119631 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(SOD1*L126Z)45Dbo/0 | involves: C3H/HeJ * C57BL/6J | J:219482 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(SOD1*L126Z)#Deng/0 | involves: C57BL/6 * SJL | J:109458 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(Thy1-DCTN1*G59S)M2Pcw/? | involves: C57BL/6 * SJL | J:132857 | View | ||||
amyotrophic lateral sclerosis type 1 |
Tg(Thy1-SOD1*G93A)T1Hgrd/0 Tg(Thy1-SOD1*G93A)T3Hgrd/0 |
involves: C57BL/6 * CBA * FVB | J:134095 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(Thy1-SOD1*G93A)T3Hgrd/Tg(Thy1-SOD1*G93A)T3Hgrd | involves: C57BL/6 * CBA * FVB | J:134095 | View | ||||
arrhythmogenic right ventricular dysplasia 9 | Tg(Myh6-Pkp2*/mRuby)4Rbrug/0 | involves: C57BL/6 * DBA/2 | J:237859 | View | ||||
arrhythmogenic right ventricular dysplasia 9 |
Tg(Myh6-Pkp2*/mRuby)4Rbrug/0 Tg(Myh6-Pkp2*/mRuby)5Rbrug/0 |
involves: C57BL/6 * DBA/2 | J:237859 | View | ||||
arrhythmogenic right ventricular dysplasia 9 | Tg(Myh6-Pkp2*/mRuby)5Rbrug/0 | involves: C57BL/6 * DBA/2 | J:237859 | View | ||||
arrhythmogenic right ventricular dysplasia 12 | Tg(Myh6-JUP*)1Dpju/0 | FVB/N-Tg(Myh6-JUP*)1Dpju | J:235770 | View | ||||
autosomal dominant hypophosphatemic rickets | Tg(APOE-FGF23*R176Q)#Ack/0 | involves: C57BL/6J * CBA | J:93981 | View | ||||
autosomal dominant keratitis-ichthyosis-deafness syndrome |
Tg(KRT14-rtTA)F42Efu/0 Tg(tetO-GJB2*G45E,-EGFP)#Tww/0 |
involves: FVB/N * SKH1 | J:220589 | View | ||||
autosomal dominant limb-girdle muscular dystrophy type 1 | Tg(Ckm-DNAJB6_ib*F93L)#Ccwe/0 | B6.Cg-Tg(Ckm-DNAJB6_ib*F93L)#Ccwe | J:226488 | View | ||||
Axenfeld-Rieger syndrome type 1 | Tg(Kera-PITX2*A)AHjal/0 | involves: C57BL/6 * CBA | J:93634 | View | ||||
Axenfeld-Rieger syndrome type 1 | Tg(Kera-PITX2*A)BHjal/0 | involves: C57BL/6 * CBA | J:93634 | View | ||||
CADASIL 1 | Tg(Notch3*R169C)88Bbb/0 | involves: FVB/N | J:220006 | View | ||||
Carney complex |
Tg(CMV-tTA)3Bjd/0 Tg(tetO-Prkar1a*x2as)1Stra/0 |
involves: C57BL/6 * NMRI * SJL | J:95465 | View | ||||
cataract 2 multiple types | Tg(CRYBB1-CRYGC*)#Jfhe/? | involves: FVB/N | J:181433 | View | ||||
Charcot-Marie-Tooth disease axonal type 2F | Tg(Thy1-HSPB1*S135F)#Lvdb/0 | involves: FVB/N | J:174508 | View | ||||
Charcot-Marie-Tooth disease type 1A | Tg(PMP22)C3Fbas/? | B6.Cg-Tg(PMP22)C3Fbas | J:237901 | View | ||||
Charcot-Marie-Tooth disease type 1A | Tg(PMP22)C22Clh/0 | involves: C57BL/6J * CBA/Ca | J:78221, J:76795 | View | ||||
Charcot-Marie-Tooth disease type 1A | Tg(PMP22)C61Clh/0 | B6.Cg-Tg(PMP22)C61Clh | J:158350 | View | ||||
Charcot-Marie-Tooth disease type 1C | Tg(CMV-LITAF*W116G)#Lli/Tg(CMV-LITAF*W116G)#Lli | FVB-Tg(CMV-LITAF*W116G)#Lli | J:194981 | View | ||||
Charcot-Marie-Tooth disease type 2A2A | Tg(Eno2-MFN2*R94Q)L51Ugfm/0 | involves: C57BL/6 * C57BL/6J * DBA/2 | J:158936 | View | ||||
Charcot-Marie-Tooth disease type 2A2A | Tg(Eno2-MFN2*R94Q)L51Ugfm/0 | involves: C57BL/6 * DBA/2 | J:173431 | View | ||||
Charcot-Marie-Tooth disease type 2A2A | Tg(Eno2-MFN2*R94Q)L87Ugfm/Tg(Eno2-MFN2*R94Q)L87Ugfm | involves: C57BL/6 * DBA/2 | J:173431 | View | ||||
Charcot-Marie-Tooth disease type 2E | Tg(NEFL*E397K)#Milg/0 | Not Specified | J:173771 | View | ||||
Charcot-Marie-Tooth disease type 2E |
Tg(tetO-NEFL)173.2Jpj/0 Tg(THY1-tTA)177Jpj/0 |
involves: C3H * C57BL/6 | J:160704 | View | ||||
dentatorubral-pallidoluysian atrophy | Tg(ATN1*)Q129Stsu/0 | involves: 129S/SvEv * C57BL/6J | J:144379 | View | ||||
dentatorubral-pallidoluysian atrophy | Tg(Eno2-ATN1)3Tx/Tg(Eno2-ATN1)3Tx | B6.Cg-Tg(Eno2-ATN1)3Tx | J:112706 | View | ||||
dentatorubral-pallidoluysian atrophy | Tg(Eno2-ATN1)14Tx/0 | B6.Cg-Tg(Eno2-ATN1)14Tx | J:112706 | View | ||||
dentatorubral-pallidoluysian atrophy | Tg(Prnp-ATN1)124Dbo/? | involves: C3H * C57BL/6 | J:70362 | View | ||||
dentatorubral-pallidoluysian atrophy | Tg(Prnp-ATN1)150Dbo/? | involves: C3H * C57BL/6 | J:70362 | View | ||||
DiGeorge syndrome | Del(16Es2el-Ufd1l)217Bld/+ | involves: 129S7/SvEvBrd * C57BL/6 | J:57757 | View | ||||
dilated cardiomyopathy 1A | Tg(Myh6-LMNA*E82K)35Lizh/0 | involves: C57BL/6J | J:167734 | View | ||||
dilated cardiomyopathy 1C | Tg(Myh6-LDB3*S196L)93Mva/0 | involves: C57BL/6J | J:243711 | View | ||||
dilated cardiomyopathy 1D | Tg(Myh6-TNNT2*R141W)#Ajm/0 | involves: C3H * C57BL/6 * ICR | J:161899 | View | ||||
dilated cardiomyopathy 1D | Tg(Myh6-TNNT2*R141W)#Lian/0 | involves: C57BL/6J | J:211769 | View | ||||
dilated cardiomyopathy 1E |
Tg(Myh6-rtTA)8585Jam/0 Tg(Myh6*/tetO-SCN5A*F1759A)#Marx/0 |
involves: C57BL/6 * CBA * FVB/NTac | J:229825 | View | ||||
dilated cardiomyopathy 1R | Tg(Myh6-ACTC1*E361G)361.20Sbm/0 | Not Specified | J:242344 | View | ||||
dilated cardiomyopathy 1Y | Tg(Myh6-Tpm1*D230N)HJcf/0 | B6.FVB-Tg(Myh6-Tpm1*D230N)HJcf | J:243724 | View | ||||
familial encephalopathy with neuroserpin inclusion bodies | Tg(Thy1-SERPINI1*G392E)333Icka/0 | involves: C57BL * CD-1 * DBA | J:144649 | View | ||||
familial encephalopathy with neuroserpin inclusion bodies | Tg(Thy1-SERPINI1*G392E)333Icka/Tg(Thy1-SERPINI1*G392E)333Icka | involves: C57BL * CD-1 * DBA | J:144649 | View | ||||
Feingold syndrome | Mirc1tm1.2Tyj/Mirc1+ | involves: 129S4/SvJae * C57BL/6 | J:188762 | View | ||||
fibrodysplasia ossificans progressiva | Tg(CAG-LacZ,-ACVR1*,-EGFP)35-1Mis/0 | involves: C57BL/6 * DBA/2 | J:142253 | View | ||||
Finnish type amyloidosis | Tg(Ckm-GSN*D187N)AJewe/0 | C57BL/6J-Tg(Ckm-GSN*D187N)AJewe | J:150825 | View | ||||
Finnish type amyloidosis | Tg(Ckm-GSN*D187N)AJewe/Tg(Ckm-GSN*D187N)AJewe | C57BL/6J-Tg(Ckm-GSN*D187N)AJewe | J:150825 | View | ||||
Grn-related frontotemporal lobar degeneration with Tdp43 inclusions | Tg(Prnp-TARDBP)3cPtrc/Tg(Prnp-TARDBP)3cPtrc | C57BL/6-Tg(Prnp-TARDBP)3cPtrc | J:163231 | View | ||||
Grn-related frontotemporal lobar degeneration with Tdp43 inclusions | Tg(TARDBP)#Jpj/0 | involves: C3H * C57BL/6 | J:195184 | View | ||||
Grn-related frontotemporal lobar degeneration with Tdp43 inclusions | Tg(TARDBP*A315T)#Jpj/0 | involves: C3H * C57BL/6 | J:195184 | View | ||||
Grn-related frontotemporal lobar degeneration with Tdp43 inclusions | Tg(TARDBP*G348C)#Jpj/0 | involves: C3H * C57BL/6 | J:195184 | View | ||||
Grn-related frontotemporal lobar degeneration with Tdp43 inclusions | Tg(Thy1-TARDBP*)BOddo/0 | C57BL/6-Tg(Thy1-TARDBP*)BOddo | J:180165 | View | ||||
Grn-related frontotemporal lobar degeneration with Tdp43 inclusions | Tg(Thy1-TARDBP*)BOddo/Tg(Thy1-TARDBP*)BOddo | C57BL/6-Tg(Thy1-TARDBP*)BOddo | J:223932 | View | ||||
hyperekplexia 1 | Tg(Thy1-GLRA1*R271Q)300Wha/0 | involves: C57BL/6 * DBA/2 | J:76009 | View | ||||
hyperekplexia 1 | Tg(Thy1-GLRA1*R271Q)382Wha/Tg(Thy1-GLRA1*R271Q)382Wha | involves: C57BL/6 * DBA/2 | J:76009 | View | ||||
long QT syndrome 1 | Tg(Myh6-KCNQ1_i2)H02Desc/0 | involves: FVB | J:132483 | View | ||||
long QT syndrome 1 | Tg(Myh6-KCNQ1_i2)H05Desc/0 | involves: FVB | J:211437 | View | ||||
Machado-Joseph disease | Tg(ATXN3*)67.2Cce/0 | involves: C57BL/6 * CBA | J:76495 | View | ||||
Machado-Joseph disease |
Tg(ATXN3*)67.2Cce/0 Tg(ATXN3*)84.2Cce/0 |
involves: C57BL/6 * CBA | J:76495 | View | ||||
Machado-Joseph disease | Tg(ATXN3*)84.2Cce/0 | involves: C57BL/6 * CBA | J:76495 | View | ||||
Machado-Joseph disease | Tg(ATXN3*)84.2Cce/Tg(ATXN3*)84.2Cce | involves: C57BL/6 * CBA | J:76495 | View | ||||
Machado-Joseph disease | Tg(CMV-ATXN3*94Q)94Pama/0 | B6.FVB-Tg(CMV-ATXN3*94Q)94Pama | J:163032 | View | ||||
Machado-Joseph disease | Tg(CMV-ATXN3*94Q)94Pama/Tg(CMV-ATXN3*94Q)94Pama | B6.FVB-Tg(CMV-ATXN3*94Q)94Pama | J:163032 | View | ||||
Machado-Joseph disease | Tg(CMV-ATXN3*135Q)CPama/0 | C57BL/6-Tg(CMV-ATXN3*135Q)CPama | J:222991 | View | ||||
Machado-Joseph disease | Tg(Htt-ATXN3*148Q)3746Thsc/0 | involves: C57BL/6N | J:156912 | View | ||||
Machado-Joseph disease | Tg(Pcp2-ATXN3*69Q)bHirai/0 | Not Specified | J:136101 | View | ||||
Machado-Joseph disease | Tg(Prnp-ATXN3*70Q)70.61Olri/0 | involves: C57BL/6N | J:122993 | View | ||||
Machado-Joseph disease | Tg(Prnp-ATXN3*79Q)#Hlw/0 | FVB/N-Tg(Prnp-ATXN3*79Q)#Hlw | J:138381 | View | ||||
Machado-Joseph disease | Tg(Prnp-ATXN3*148Q)148.19Olri/0 | involves: C57BL/6N | J:122993 | View | ||||
Machado-Joseph disease | Tg(Prnp-ATXN3*148Q)NLS.28Olri/0 | involves: C57BL/6N | J:122993 | View | ||||
maturity-onset diabetes of the young type 3 | Tg(Ins2-Hnf1a)#Cbw/0 | involves: C57BL/6 * CBA/J | J:134757 | View | ||||
maturity-onset diabetes of the young type 3 | Tg(Ins2-TCF1*P291)2Kya/0 | involves: C57BL/6 * SJL | J:73760 | View | ||||
myofibrillar myopathy 3 | Tg(ACTA1-MYOT*T57I)71Mah/? | involves: C57BL/6 * SJL | J:110377 | View | ||||
myofibrillar myopathy 6 | Tg(Myh6-BAG3*P209L)#Mswi/0 | involves: C57BL/6 * DBA/2 | J:234278 | View | ||||
neurodegeneration with brain iron accumulation 3 | Tg(PGK1-FTL*)#Sle/0 | B6J.FVB-Tg(PGK1-FTL*)#Sle | J:226967 | View | ||||
neurodegeneration with brain iron accumulation 3 | Tg(Prnp-FTL*)4Ruvi/Tg(Prnp-FTL*)4Ruvi | B6.C3Fe-Tg(Prnp-FTL*)4Ruvi | J:131053 | View | ||||
Noonan syndrome 1 |
H2az2Tg(Wnt1-cre)11Rth/H2az2+ Tg(CAG-cat,-Ptpn11*Q97R)1Rbns/0 |
involves: C57BL/6J * CBA/J * FVB/N | J:153094 | View | ||||
Noonan syndrome 1 |
Tg(CAG-cat,-Ptpn11*Q97R)1Rbns/0 Tg(Tek-cre)12Flv/0 |
involves: C3H * C57BL/6 * FVB/N | J:142212 | View | ||||
Noonan syndrome with multiple lentigines |
Tg(CAG-cat,-Ptpn11*Q510E)#Krnz/0 Tg(Tek-cre)1Ywa/0 |
involves: C57BL/6 * FVB/N * SJL | J:237450 | View | ||||
osteogenesis imperfecta type 1 | Tg(COL1A1)73Prc/0 | involves: FVB/N | J:146429 | View | ||||
Parkinson's disease 1 | Tg(PDGFB-SNCA)4Ema/0 | involves: C57BL/6 * DBA/2 | J:60638, J:166985 | View | ||||
Parkinson's disease 1 | Tg(PDGFB-SNCA*A53T)8Ema/0 | Not Specified | J:226922 | View | ||||
Parkinson's disease 1 | Tg(PDGFB-SNCA/EGFP)78Ema/0 | involves: C57BL/6 * DBA/2 | J:238692 | View | ||||
Parkinson's disease 1 | Tg(Prnp-SNCA*A53T)25Mkle/0 | involves: C3H/HeJ * C57BL/6J | J:77344 | View | ||||
Parkinson's disease 1 | Tg(Prnp-SNCA*A53T)83Vle/0 | involves: C3H * C57BL/6 | J:76657 | View | ||||
Parkinson's disease 1 | Tg(Prnp-SNCA*A53T)83Vle/Tg(Prnp-SNCA*A53T)83Vle | involves: C3H * C57BL/6 | J:76657 | View | ||||
Parkinson's disease 1 | Tg(Prnp-SNCA*A53T)AAub/? | involves: FVB/N | J:216589 | View | ||||
Parkinson's disease 1 | Tg(Prnp-SNCA*A53T)AAub/Tg(Prnp-SNCA*A53T)AAub | involves: FVB/N | J:181820, J:185489 | View | ||||
Parkinson's disease 1 | Tg(SNCA)ARyot/0 | C57BL/6J-Tg(SNCA)ARyot | J:185434 | View | ||||
Parkinson's disease 1 | Tg(SNCA*E46K)3Elan/? | involves: C57BL/6 * SJL | J:200740 | View | ||||
Parkinson's disease 1 | Tg(Snca-SNCA)#Galt/? | involves: C57BL/6 * DBA/2 | J:199939 | View | ||||
Parkinson's disease 1 | Tg(Th-SNCA*)1702Yosh/0 | involves: C3H * C57BL/6J | J:125149 | View | ||||
Parkinson's disease 1 | Tg(Thy1-SNCA)61Ema/0 | involves: C57BL/6 * DBA/2 | J:137490 | View | ||||
Parkinson's disease 1 | Tg(Thy1-SNCA*)#Ztzh/0 | involves: C57BL/6J | J:313970 | View | ||||
Parkinson's disease 1 | Tg(Thy1-SNCA*A30P)18Pjk/Tg(Thy1-SNCA*A30P)18Pjk | involves: C57BL/6 | J:80181 | View | ||||
Parkinson's disease 1 | Tg(THY1-SNCA*A53T)M53Sud/0 | B6.Cg-Tg(THY1-SNCA*A53T)M53Sud/J | J:212732 | View | ||||
Parkinson's disease 1 | Tg(Thy1-SNCA*E57K)16Ema/0 | involves: C57BL/6 * DBA/2 | J:236596 | View | ||||
Parkinson's disease 8 | Tg(PDGFB-LRRK2*G2019S)32Hlw/? | FVB/N-Tg(PDGFB-LRRK2*G2019S)32Hlw | J:204793 | View | ||||
Parkinson's disease 8 | Tg(PDGFB-LRRK2*R1441C)31Hlw/0 | FVB/N-Tg(PDGFB-LRRK2*R1441C)31Hlw | J:229559 | View | ||||
PCWH syndrome | Tg(Venus/SOX10*)55Kein/0 | involves: C3H/He * C57BL/6 | J:227442 | View | ||||
PCWH syndrome | Tg(Venus/SOX10*)55Kein/Tg(Venus/SOX10*)55Kein | involves: C3H/He * C57BL/6 | J:227442 | View | ||||
Perry syndrome | Tg(Thy1-DCTN1*G71A)#Ytsu/0 | involves: C57BL/6J | J:258253 | View | ||||
polycystic kidney disease 2 | Tg(CAG-PKD2)#Hwl/? | involves: FVB/NJ | J:148377 | View | ||||
progeria |
Tg(KRT5-tTA)1216Glk/0 Tg(tetO-LMNA*G608G,-EGFP)VF1-07Maer/0 |
involves: FVB/N | J:145312 | View | ||||
progeria | Tg(LMNA*G608G)HClns/? | C57BL/6-Tg(LMNA*G608G)HClns/J | J:107176 | View | ||||
pseudoachondroplasia | Tg(Col2a1-rtTA,tetO-COMP*)2Jath/0 | C57BL/6-Tg(Col2a1-rtTA,tetO-COMP*)2Jath | J:152756, J:233238 | View | ||||
retinitis pigmentosa 4 |
Ntrk3tm1.1Tes/Ntrk3+ Tg(RHO*P347S)A1Tili/0 |
involves: 129S1/Sv * C57BL/6J * FVB/N | J:262975 | View | ||||
retinitis pigmentosa 4 | Tg(RHO*P347S)A1Tili/0 | involves: C57BL/6J * FVB/N | J:262975 | View | ||||
retinitis pigmentosa 4 | Tg(RHO-P23H)DTpd/? | involves: C57BL/6 * DBA/2 | J:76722 | View | ||||
spinocerebellar ataxia type 1 | Tg(Pcp2-ATXN1*82Q)5Horr/0 | involves: FVB/N | J:166951 | View | ||||
spinocerebellar ataxia type 1 |
Tg(Pcp2-tTA)3Horr/0 Tg(tetO-ATXN1*82Q)#Horr/Tg(tetO-ATXN1*82Q)#Horr |
involves: FVB/N | J:95453 | View | ||||
spinocerebellar ataxia type 2 | Tg(ATXN2*72Q)#Plt/0 | FVB/N-Tg(ATXN2*72Q)#Plt | J:224692 | View | ||||
spinocerebellar ataxia type 2 | Tg(Pcp2-ATXN2*127Q)#Plt/0 | involves: C57BL/6 * DBA/2 | J:191127 | View | ||||
spinocerebellar ataxia type 5 |
Tg(Pcp2-tTA)3Horr/0 Tg(tetO-SPTBN2*)#Lpwr/0 |
involves: FVB/N | J:215593 | View | ||||
spinocerebellar ataxia type 7 | Tg(GFAP-ATXN7*92Q)2521Als/0 | involves: C3H/HeJ * C57BL/6J | J:113150 | View | ||||
spinocerebellar ataxia type 7 | Tg(GFAP-ATXN7*92Q)2542Als/0 | involves: C3H/HeJ * C57BL/6J | J:113150 | View | ||||
spinocerebellar ataxia type 7 | Tg(Pcp2-SCA7)P7EJman/0 | involves: C57BL/6 * SJL | J:65411 | View | ||||
spinocerebellar ataxia type 7 | Tg(Prnp-ATXN7*92Q)1963Als/0 | B6J.Cg-Tg(Prnp-ATXN7*92Q)1963Als | J:222402 | View | ||||
spinocerebellar ataxia type 7 | Tg(Prnp-ATXN7*92Q)6076Als/0 | involves: C3H/HeJ * C57BL/6 | J:71971, J:77530, J:113150 | View | ||||
spinocerebellar ataxia type 7 | Tg(RHO-SCA7)R7EJman/0 | involves: C57BL/6 * SJL | J:65411 | View | ||||
spinocerebellar ataxia type 10 | Tg(Prnp-lacZ/ATXN10*)#Teas/0 | involves: FVB/N | J:222081 | View | ||||
spinocerebellar ataxia type 14 |
Tg(Pcp2-tTA)3Horr/0 Tg(tetO-PRKCG*S361G,-GFP)3Jpka/0 |
involves: FVB/N | J:218354 | View | ||||
spinocerebellar ataxia type 17 | Tg(Pcp2-TBP*)69Hmhl/0 | involves: FVB/N | J:174239 | View | ||||
spinocerebellar ataxia type 17 | Tg(Prnp-TBP*)71-16Xjl/0 | FVB/N-Tg(Prnp-TBP*)71-16Xjl | J:130775 | View | ||||
spinocerebellar ataxia type 17 | Tg(Prnp-TBP*)71-27Xjl/0 | FVB/N-Tg(Prnp-TBP*)71-27Xjl | J:130775 | View | ||||
spinocerebellar ataxia type 17 | Tg(Prnp-TBP*)105Xjl/0 | FVB/N-Tg(Prnp-TBP*)105Xjl | J:130775 | View | ||||
Stargardt disease | Tg(RBP3-ELOVL4*)1Kzh/0 | C57BL/6-Tg(RBP3-ELOVL4*)1Kzh | J:97173 | View | ||||
Stargardt disease | Tg(RBP3-ELOVL4*)2Kzh/0 | C57BL/6-Tg(RBP3-ELOVL4*)2Kzh | J:97173 | View | ||||
Stargardt disease | Tg(RBP3-ELOVL4*)3Kzh/0 | C57BL/6-Tg(RBP3-ELOVL4*)3Kzh | J:97173 | View | ||||
torsion dystonia 1 | Tg(CMV-TOR1A*)1Nush/0 | involves: C3H * C57BL/6 | J:98716 | View | ||||
torsion dystonia 1 | Tg(CMV-TOR1A*)2Nush/0 | involves: C3H * C57BL/6 | J:98716 | View | ||||
torsion dystonia 1 | Tg(Eno2-TOR1A*)13Shas/0 | involves: C3H * C57BL/6J | J:95447 | View | ||||
transthyretin amyloidosis |
Hsf1tm1Ijb/Hsf1tm1Ijb Tg(TTR-V30M)15Imeg/0 |
involves: 129S6/SvEvTac * BALB/c * C57BL/6 | J:156658 | View | ||||
transthyretin amyloidosis | Tg(TTR-V30M)15Imeg/0 | involves: C57BL/6 | J:260683 | View | ||||
transthyretin amyloidosis | Tg(TTR-V30M)15Imeg/0 | Not Specified | J:80880 | View | ||||
tuberous sclerosis |
Emx1tm1(cre)Ito/Emx1+ Tg(CAG-Mtor*)#Atai/0 |
involves: 129P2/OlaHsd * C57BL/6 * DBA/2 * ICR | J:211789 | View | ||||
Additional Complex Models | abdominal obesity-metabolic syndrome |
Ay/a Apoetm1Unc/Apoetm1Unc |
involves: 129P2/OlaHsd * C57BL/6J * KK/TaJcl | J:177084 | View | |||
abdominal obesity-metabolic syndrome |
Apoetm1Unc/Apoetm1Unc Cyp19a1tm1Esi/Cyp19a1tm1Esi |
involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 | J:184647 | View | ||||
age related macular degeneration |
Abca4tm1Kpal/Abca4tm1Kpal Rdh8tm1Kpal/Rdh8tm1Kpal |
involves: 129 | J:213619 | View | ||||
age related macular degeneration 1 |
Cptm1Hrs/Cptm1Hrs Hephsla/Y |
involves: 129X1/SvJ * C57BL/6 | J:136925 | View | ||||
Alzheimer's disease 3 |
Tg(APP695)3Dbo/0 Tg(PSEN1)5Dbo/0 |
involves: C3H/HeJ * C57BL/6J | J:43788 | View | ||||
amyotrophic lateral sclerosis type 1 |
Tg(SOD1)2Gur/0 Tg(SOD1*A4V)A1073Gur/0 |
involves: C57BL/6 * SJL | J:109458 | View | ||||
Birt-Hogg-Dube syndrome |
Fnip1tm1.2Baba/Fnip1+ Fnip2tm1.2Lss/Fnip2tm1.2Lss |
involves: C57BL/6 | J:220672 | View | ||||
brachydactyly type A1 | ShhDsh/Shh+ | B10Rl.Cg-ShhDsh | J:97323 | View | ||||
CADASIL 1 |
Gt(ROSA)26Sortm3(NOTCH3*R1031C)Sat/Gt(ROSA)26Sor+ Tg(Tagln-cre)1Her/0 |
involves: 129S2/SvPas * 129S6/SvEvTac * C57BL/6 * SJL | J:171887 | View | ||||
Charcot-Marie-Tooth disease type 2A2A |
Gt(ROSA)26Sortm1(CAG-MFN2*T105M)Dple/Gt(ROSA)26Sor+ Tg(Nes-cre)1Kln/0 |
involves: C57BL/6 * SJL | J:251584 | View | ||||
CINCA Syndrome |
Prkacatm1Gsm/Prkaca+ Prkar1atm1.1Lsk/Prkar1a+ |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:166728 | View | ||||
dilated cardiomyopathy 1A |
H2-Ab1b-tm1Gru/H2-Ab1b-tm1Gru Tg(CD2-CD4,HLA-DQA1,HLA-DQB1)1Ell/Tg(CD2-CD4,HLA-DQA1,HLA-DQB1)1Ell |
NOD.Cg-H2-Ab1b-tm1Gru Tg(CD2-CD4,HLA-DQA1,HLA-DQB1)1Ell | J:86540 | View | ||||
hereditary spastic paraplegia 4 | Gt(ROSA)26Sortm1.1(CAG-SPAST*C448Y)Baas/Gt(ROSA)26Sor+ | involves: C57BL/6N | J:273408 | View | ||||
hereditary spastic paraplegia 4 | Gt(ROSA)26Sortm1.1(CAG-SPAST*C448Y)Baas/Gt(ROSA)26Sortm1.1(CAG-SPAST*C448Y)Baas | involves: C57BL/6N | J:273408 | View | ||||
hyper IgE recurrent infection syndrome 1 |
Igh-Jtm1Mcdl/Igh-Jtm1Mcdl Igk-Jtm1Mcdl/Igk-Jtm1Mcdl Rag1tm1Mom/Rag1tm1Mom Tg(DO11.10)10Dlo/? |
involves: 129S/Sv * BALB/c * C3H * C57BL/6 | J:100072 | View | ||||
Machado-Joseph disease |
Prnptm1Cwe/Prnptm1Cwe Tg(Prnp-tTA)F959Sbp/0 Tg(tetO-ATXN3)2904Olri/Tg(tetO-ATXN3)2904Olri |
involves: 129S7/SvEvBrd * C57BL/6 * FVB | J:154079 | View | ||||
Machado-Joseph disease |
Prnptm1Cwe/Prnptm1Cwe Tg(Prnp-tTA)F959Sbp/Tg(Prnp-tTA)F959Sbp Tg(tetO-ATXN3)2904Olri/0 |
involves: 129S7/SvEvBrd * C57BL/6 * FVB | J:154079 | View | ||||
Machado-Joseph disease |
Prnptm1Cwe/Prnptm1Cwe Tg(Prnp-tTA)F959Sbp/Tg(Prnp-tTA)F959Sbp Tg(tetO-ATXN3)2904Olri/Tg(tetO-ATXN3)2904Olri |
involves: 129S7/SvEvBrd * C57BL/6 * FVB | J:154079 | View | ||||
maturity-onset diabetes of the young |
Foxo1tm1Rdp/Foxo1tm1Rdp Foxo3tm1Rdp/Foxo3tm1Rdp Foxo4tm1Rdp/Foxo4tm1Rdp Tg(Ins2-cre)23Herr/0 |
involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J * CBA/J | J:215526 | View | ||||
neurofibromatosis 1 |
Krastm4Tyj/Kras+ Ptentm1Hwu/Pten+ Tg(Gfap-cre)77.6Mvs/0 |
involves: 129S4/SvJae * BALB/c * C57BL/6NHsd | J:154673 | View | ||||
Parkinson's disease 1 | 2310039L15RikTg(Prnp-SNCA*A53T)23Mkle/2310039L15Rik+ | involves: C3H/HeJ * C57BL/6J | J:77344 | View | ||||
Parkinson's disease 1 |
Gt(ROSA)26Sortm2(SNCA*119)Djmo/Gt(ROSA)26Sortm2(SNCA*119)Djmo 7630403G23RikTg(Th-cre)1Tmd/7630403G23Rik+ |
involves: 129 * C57BL/6 | J:150777 | View | ||||
Parkinson's disease 1 |
Gt(ROSA)26Sortm2(SNCA*119)Djmo/Gt(ROSA)26Sortm2(SNCA*119)Djmo 7630403G23RikTg(Th-cre)1Tmd/7630403G23Rik+ |
involves: 129 * C57BL/6 * SJL | J:150777 | View | ||||
Parkinson's disease 8 | Khdrbs2Tg(LRRK2*R1441G)135Cjli/Khdrbs2+ | FVB-Khdrbs2Tg(LRRK2*R1441G)135Cjli | J:149135 | View | ||||
Parkinson's disease 8 | Khdrbs2Tg(LRRK2*R1441G)135Cjli/Khdrbs2+ | FVB/N-Khdrbs2Tg(LRRK2*R1441G)135Cjli/J | J:204940 | View | ||||
spondyloepiphyseal dysplasia congenita |
Gt(ROSA)26Sortm5(ACTB-tTA)Luo/Gt(ROSA)26Sor+ Tg(Col2a1-cre)1Bhr/0 Tg(tetO/CMV-Col2a1*R992C,-GFP)#Afe/0 |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6J * SJL | J:216945 | View |
No similarity to the expected human disease phenotype was found.
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Disease Term | Allelic Composition | Genetic Background | Reference | Phenotypes | ||||
NOT Models | Alzheimer's disease 3 | Psen1tm1Psgh/Psen1tm1Psgh | Not Specified | J:66016 | View | |||
autosomal dominant nocturnal frontal lobe epilepsy 1 | Chrna4tm1Dra/Chrna4tm1Dra | involves: 129S4/SvJae * C57BL/6 | J:64208, J:97020 | View | ||||
autosomal dominant nonsyndromic deafness 2A | Gjb3tm1Kwi/Gjb3tm1Kwi | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:68014 | View | ||||
autosomal dominant nonsyndromic deafness 15 | Pou4f3tm1Rsd/Pou4f3+ | involves: 129S4/SvJae * C57BL/6 | J:57149 | View | ||||
autosomal dominant nonsyndromic deafness 65 |
Cdh23Ahl+/Cdh23Ahl+ Tbc1d24em4Tbf/Tbc1d24em4Tbf |
B6.Cg-Cdh23Ahl+ Tbc1d24em4Tbf | J:299025 | View | ||||
autosomal dominant nonsyndromic deafness 65 | Tbc1d24em4Tbf/Tbc1d24em4Tbf | C57BL/6J-Tbc1d24em4Tbf | J:299025 | View | ||||
CADASIL 1 | Notch3tm1Grid/Notch3tm1Grid | involves: 129S1/Sv * C57BL/6 | J:227333 | View | ||||
CADASIL 1 | Notch3tm1Ul/Notch3+ | Not Specified | J:95927 | View | ||||
CADASIL 1 | Notch3tm1Ul/Notch3tm1Ul | Not Specified | J:95927 | View | ||||
cherubism |
Sh3bp2tm1Bjro/Sh3bp2tm1Bjro Tnftm1Gkl/Tnftm1Gkl |
involves: 129S/SvEv * 129S4/SvJae * BALB/cJ * C57BL/6J | J:117880 | View | ||||
complex cortical dysplasia with other brain malformations 7 | Tuba8tm1.2Ctpd/Tuba8tm1.2Ctpd | involves: 129P2/OlaHsd * C57BL/6J | J:248203 | View | ||||
congenital dyserythropoietic anemia type IIIa | Kif23tm1.1Igo/Kif23+ | involves: C57BL/6 * C57BL/6NTac | J:321429 | View | ||||
congenital dyserythropoietic anemia type IIIa | Kif23tm1.1Igo/Kif23tm1.1Igo | involves: C57BL/6 * C57BL/6NTac | J:321429 | View | ||||
developmental and epileptic encephalopathy 14 | Kcnt1em1Pqt/Kcnt1+ | C57BL/6J-Kcnt1em1Pqt | J:333512 | View | ||||
dilated cardiomyopathy 1D | Tnnt2tm1Mmto/Tnnt2+ | involves: 129S/SvEv | J:141967 | View | ||||
dysplastic nevus syndrome | Cdkn2atm1Rdp/Cdkn2atm1Rdp | involves: 129/Sv * C57BL/6 * SJL | J:53805 | View | ||||
familial medullary thyroid carcinoma | Rettm2.1Cos/Ret+ | involves: 129S1/Sv * C57BL/6J * FVB/N | J:60659 | View | ||||
familial medullary thyroid carcinoma | Rettm2.1Cos/Rettm2.1Cos | involves: 129S1/Sv * C57BL/6J * FVB/N | J:60659 | View | ||||
focal segmental glomerulosclerosis 1 | Tg(CMV-Plaur*)19Lbh/0 | FVB/N-Tg(CMV-Plaur*)19Lbh | J:217443 | View | ||||
Hailey-Hailey disease | Atp2c1tm1Ges/Atp2c1+ | involves: 129X1/SvJ * Black Swiss | J:124662 | View | ||||
hereditary spastic paraplegia 8 | Washc5tm1.2Cbee/Washc5+ | involves: C57BL/6 | J:266630 | View | ||||
holoprosencephaly 4 | Tgif1tm1.1Caw/Tgif1tm1.1Caw | involves: C57BL/6 * FVB/N | J:97642 | View | ||||
mandibulofacial dysostosis, Guion-Almeida type | Eftud2em1Lajm/Eftud2+ | involves: C57BL/6 | J:278323 | View | ||||
mandibulofacial dysostosis, Guion-Almeida type | Eftud2em2Lajm/Eftud2+ | involves: CD-1 * FVB/N | J:278323 | View | ||||
Mowat-Wilson syndrome | Zeb2tm1.2Yhi/Zeb2+ | involves: 129S1/Sv * 129X1/SvJ * CD-1 | J:82084 | View | ||||
multiple endocrine neoplasia type 2B | Rettm1Cos/Rettm2.1Cos | involves: 129S/SvEv * 129S1/Sv * C57BL/6J * FVB/N * MF1 | J:60659 | View | ||||
myofibrillar myopathy 3 | Myottm1.1Moza/Myottm1.1Moza | involves: 129S1/Sv * 129X1/SvJ * ICR | J:117709 | View | ||||
neurofibromatosis 1 | Nf1tm1Tyj/Nf1+ | involves: 129S2/SvPas * C57BL/6 | J:18542 | View | ||||
Noonan syndrome 1 | Ptpn11tm1Paw/Ptpn11tm1Paw | involves: 129S1/Sv * 129X1/SvJ * CD-1 | J:43740 | View | ||||
Noonan syndrome 1 | Ptpn11tm1Rbn/Ptpn11+ | involves: 129 * Black Swiss | J:35137 | View | ||||
Noonan syndrome 1 | Ptpn11tm1Rbn/Ptpn11tm1Rbn | involves: 129 * Black Swiss | J:35137 | View | ||||
osteogenesis imperfecta type 5 | Ifitm5em1Pmof/Ifitm5+ | involves: CD-1 | J:255349 | View | ||||
paraganglioma |
Sdhctm1c(EUCOMM)Wtsi/Sdhctm1c(EUCOMM)Wtsi Gt(ROSA)26Sortm1.1(rtTA,tetO-cre)Bkmn/Gt(ROSA)26Sor+ |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6N | J:284745 | View | ||||
paraganglioma | Sdhdtm1Jlob/Sdhd+ | involves: 129X1/SvJ | J:95252 | View | ||||
paraganglioma | Sdhdtm1Jlob/Sdhdtm1Jlob | involves: 129X1/SvJ | J:95252 | View | ||||
paraganglioma | Sdhdtm1Jpb/Sdhd+ | either: 129P2/OlaHsd-Sdhdtm1Jpb or (involves: 129P2/OlaHsd * C57BL/6J) | J:155380 | View | ||||
progeria | Lmnatm5Lgf/Lmnatm5Lgf | involves: 129P2/OlaHsd * C57BL/6 | J:160705 | View | ||||
progeria | Lmnatm8Lgf/Lmnatm8Lgf | involves: 129P2/OlaHsd | J:167229 | View | ||||
pseudoachondroplasia | Comptm1Aol/Comptm1Aol | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:76781 | View | ||||
retinitis pigmentosa 11 | Prpf31tm1Bha/Prpf31+ | involves: 129S2/SvPas * C57BL/6J | J:158261 | View | ||||
retinitis pigmentosa 18 | Prpf3Gt(RRO284)Byg/Prpf3+ | involves: 129P2/OlaHsd * C57BL/6 | J:141780 | View | ||||
spinocerebellar ataxia type 5 | Sptbn2tm1Mjac/Sptbn2+ | involves: 129P2/OlaHsd | J:163169 | View | ||||
spinocerebellar ataxia type 17 | Tg(Prnp-TBP*)13Xjl/0 | FVB/N-Tg(Prnp-TBP*)13Xjl | J:130775 | View | ||||
Stargardt disease | Elovl4tm1Sie/Elovl4+ | involves: 129P2/OlaHsd * C57BL/6 | J:112264 | View | ||||
Stargardt disease | Elovl4tm1Sie/Elovl4tm1Sie | involves: 129P2/OlaHsd * C57BL/6 | J:112264 | View | ||||
tibial muscular dystrophy |
Capn3tm1Jsb/Capn3+ Ttntm1.1Isrd/Ttn+ |
involves: 129/Sv * 129S2/SvPas * C57BL/6 | J:165576 | View | ||||
type 1 diabetes mellitus 2 | Hk2tm1Laak/Hk2+ | involves: 129P2/OlaHsd * BALB/c * DBA/2 | J:56644 | View | ||||
Waardenburg syndrome type 3 | Pax3Sp-2H/Pax3+ | involves: C57BL/6 | J:14096 | View | ||||
Waardenburg syndrome type 3 | Pax3Sp-2H/Pax3Sp-2H | involves: 101 * C3H/He * CBA/Ca | J:46341 | View | ||||
Waardenburg syndrome type 3 | Pax3Sp-2H/Pax3Sp-2H | involves: C57BL/6 | J:14096 | View | ||||
Waardenburg syndrome type 3 | Pax3Sp-d/Pax3+ | C57BL/6J-Pax3Sp-d | J:238 | View | ||||
Waardenburg syndrome type 3 | Pax3Sp-d/Pax3Sp-d | C57BL/6J-Pax3Sp-d | J:238 | View | ||||
Williams-Beuren syndrome | Fzd9tm1Uta/Fzd9tm1Uta | involves: 129S6/SvEvTac * 129X1/SvJ | J:98133 | View |