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All mouse models of bone development disease with phenotypic similarity to the human disease
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Disease Term | Allelic Composition | Genetic Background | Reference | Phenotypes | ||||
acheiropody | Lmbr1tm1Kng/Lmbr1tm1Kng | involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA/2J | J:72166 | View | ||||
achondrogenesis type IA |
Tg(EIIa-cre)C5379Lmgd/? Trip11tm1.2Psmi/Trip11tm1.2Psmi |
involves: 129/Sv * C57BL/6 * FVB/N | J:253969 | View | ||||
achondrogenesis type IA | Trip11m1Mawa/Trip11m1Mawa | C57BL/6J-Trip11m1Mawa | J:163656 | View | ||||
achondrogenesis type IA |
Trip11tm1.1Psmi/Trip11tm1.2Psmi Gt(ROSA)26Sortm4(ACTB-tdTomato,-EGFP)Luo/? Tg(Col2a1-cre)1Bhr/? |
involves: 129/Sv * C57BL/6 * SJL/J | J:253969 | View | ||||
achondrogenesis type II | Col2a1tm1Prc/Col2a1tm1Prc | involves: 129 | J:117910 | View | ||||
achondroplasia | Fgfr3tm1.1(FGFR3*)Ytc/Fgfr3+ | involves: 129 | J:287271 | View | ||||
achondroplasia | Fgfr3tm1.1(FGFR3*)Ytc/Fgfr3tm1.1(FGFR3*)Ytc | involves: 129 | J:287271 | View | ||||
achondroplasia | Fgfr3tm1Cxd/Fgfr3tm1Cxd | involves: 129S6/SvEvTac * NIH Black Swiss | J:52438 | View | ||||
achondroplasia | Fgfr3tm1Llm/Fgfr3+ | involves: 129S2/SvPas | J:203653 | View | ||||
achondroplasia | Fgfr3tm2Wei/Fgfr3+ | involves: 129S1/Sv * 129X1/SvJ * MF1 | J:54829 | View | ||||
achondroplasia | Fgfr3tm3.1Cxd/Fgfr3+ | involves: 129S6/SvEvTac | J:69849 | View | ||||
achondroplasia | Fgfr3tm3.1Cxd/Fgfr3tm3.1Cxd | involves: 129S6/SvEvTac | J:69849 | View | ||||
achondroplasia | Fgfr3tm5.1Cxd/Fgfr3+ | involves: 129S6/SvEvTac | J:67780 | View | ||||
achondroplasia | Tg(Col2a1-Fgfr3/GH)BDor/0 | FVB/N-Tg(Col2a1-Fgfr3/GH)BDor | J:50292 | View | ||||
acrocephalosyndactylia |
Fgfr2tm1Ewj/Fgfr2+ Tg(EIIa-cre)C5379Lmgd/0 |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * FVB/N | J:101174, J:156940 | View | ||||
acrocephalosyndactylia | Fgfr2tm2.3Dsn/Fgfr2+ | involves: 129 * C57BL/6 * FVB/N | J:72517 | View | ||||
acrocephalosyndactylia |
Fgfr2tm2Cxd/Fgfr2+ Tg(EIIa-cre)C5379Lmgd/0 |
involves: 129S6/SvEvTac * C57BL/6J * FVB/N | J:228708 | View | ||||
acrocephalosyndactylia |
Fgfr2tm2Cxd/Fgfr2+ Tg(EIIa-cre)C5379Lmgd/0 |
involves: 129S6/SvEvTac * FVB/N | J:101385 | View | ||||
acrocephalosyndactylia | Fgfr2tm2Ewj/Fgfr2+ | involves: 129S1/Sv * 129X1/SvJ * C57BL/6J | J:156940 | View | ||||
acrocephalosyndactylia |
Fgfr2tm2Ewj/Fgfr2+ Tg(EIIa-cre)C5379Lmgd/0 |
B6.Cg-Fgfr2tm2Ewj Tg(EIIa-cre)C5379Lmgd | J:158773 | View | ||||
acrocephalosyndactylia | Fgfr2tm3.1Cxd/Fgfr2+ | involves: 129S6/SvEvTac * FVB/N | J:283626 | View | ||||
acrocephalosyndactylia |
Fgfr2tm3Cxd/Fgfr2+ Tg(Col2a1-cre)1Xya/0 |
involves: 129S6/SvEvTac * C57BL/6J | J:286452 | View | ||||
acrodysostosis | Prkar1atm1.1Geno/Prkar1a+ | involves: C57BL/6J | J:303060 | View | ||||
acromesomelic dysplasia, Grebe type | Gdf5Bp-5J/Gdf5+ | C57BL/6J-Gdf5Bp-5J/GrsrJ | J:200816 | View | ||||
acromesomelic dysplasia, Grebe type |
Gdf5bp-J/Gdf5bp-J Gdf6tm1Kng/Gdf6tm1Kng |
involves: 129S1/Sv * 129X1/SvJ * A/J * C57BL/6J | J:83132 | View | ||||
acromesomelic dysplasia, Hunter-Thompson type | Gdf5Bp-5J/Gdf5+ | C57BL/6J-Gdf5Bp-5J/GrsrJ | J:200816 | View | ||||
acromesomelic dysplasia, Maroteaux type | Npr2pwe/Npr2pwe | involves: C3H/HeJ * C57BL/6 * NAW/WI | J:188839 | View | ||||
acromesomelic dysplasia, Maroteaux type | Npr2slw/Npr2slw | involves: C57BL/6 * DDY | J:129973 | View | ||||
asphyxiating thoracic dystrophy 2 | Ift80Gt(AN0245)Wtsi/Ift80Gt(AN0245)Wtsi | involves: 129P2/OlaHsd | J:169236 | View | ||||
asphyxiating thoracic dystrophy 3 | Dync2h1b2b414Clo/Dync2h1b2b414Clo | C57BL/6J-Dync2h1b2b414Clo | J:175213 | 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 | ||||
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 | ||||
Carpenter syndrome | Megf8b2b288Clo/Megf8b2b288Clo | C57BL/6J-Megf8b2b288Clo | J:175213 | View | ||||
Carpenter syndrome | Megf8b2b1702.2Clo/Megf8b2b1702.2Clo | C57BL/6J-Megf8b2b1702.2Clo | J:175213 | View | ||||
chondrodysplasia with joint dislocations gPAPP type | Bpnt2tm1.2Aros/Bpnt2tm1.2Aros | B6(SJL)-Bpnt2tm1.2Aros | J:273179 | 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 | ||||
clubfoot | Pitx1tm1Rsd/Pitx1+ | involves: 129S1/Sv * 129X1/SvJ | J:175799 | View | ||||
craniosynostosis | Tg(CMV-Msx2*P7H)1Rem/0 | involves: C57BL/6 * CBA/J | J:26513 | View | ||||
craniosynostosis | Tg(Msx2)1Rem/0 | involves: C57BL/6 * CBA/J | J:26513 | View | ||||
craniosynostosis | Tg(Timp1-Msx2*P7H)1Rem/0 | involves: C57BL/6 * CBA/J | J:26513 | View | ||||
Crouzon syndrome | Fgfr2m1Sgg/Fgfr2+ | involves: C3H/HeJ * C57BL/6J | J:160674 | View | ||||
Crouzon syndrome | Fgfr2m1Sgg/Fgfr2m1Sgg | involves: C3H/HeJ * C57BL/6J | J:160674 | View | ||||
Crouzon syndrome | Fgfr2tm1Schl/Fgfr2+ | involves: 129S1/Sv | J:118299 | View | ||||
Crouzon syndrome | Fgfr2tm4Lni/Fgfr2+ | Not Specified | J:92433, J:235329 | View | ||||
Desbuquois dysplasia | Cant1tm1.1Aros/Cant1tm1.1Aros | involves: 129 * C57BL/6J | J:282272 | View | ||||
Desbuquois dysplasia | Cant1tm1.2Aros/Cant1tm1.2Aros | involves: 129 * C57BL/6J | J:282272 | View | ||||
diastrophic dysplasia | Slc26a2tm1Aros/Slc26a2tm1Aros | involves: 129S7/SvEvBrd * C57BL/6J | J:97104 | View | ||||
fibular hypoplasia and complex brachydactyly | Gdf5Bp-5J/Gdf5+ | C57BL/6J-Gdf5Bp-5J/GrsrJ | J:200816 | View | ||||
Fuhrmann syndrome | Wnt7apx-2J/Wnt7apx-2J | B6;C3Fe-Wnt7apx-2J/GrsrJ | J:188478 | View | ||||
Fuhrmann syndrome | Wnt7apx-J/Wnt7apx-J | C57BL/6J-Wnt7apx-J/GrsrJ | J:188477 | View | ||||
geleophysic dysplasia 1 |
Adamtsl2tm1c(KOMP)Wtsi/Adamtsl2tm1c(KOMP)Wtsi Tg(Prrx1-cre)1Cjt/0 |
B6.Cg-Adamtsl2tm1c(KOMP)Wtsi Tg(Prrx1-cre)1Cjt | J:280264 | 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 | ||||
hypertrichotic osteochondrodysplasia Cantu type | Abcc9em1Nich/Abcc9+ | involves: C57BL/6J * CBA/J | J:281903 | View | ||||
hypertrichotic osteochondrodysplasia Cantu type | Abcc9em1Nich/Abcc9em1Nich | involves: C57BL/6J * CBA/J | J:281903 | View | ||||
hypertrichotic osteochondrodysplasia Cantu type | Abcc9em3Nich/Abcc9+ | B6.Cg-Abcc9em3Nich | J:308986 | View | ||||
hypertrichotic osteochondrodysplasia Cantu type | Abcc9em3Nich/Abcc9em3Nich | B6.Cg-Abcc9em3Nich | J:308986 | View | ||||
hypochondroplasia | Fgfr3tm3.1Llm/Fgfr3+ | involves: C57BL/6N | J:338859 | View | ||||
microcephalic osteodysplastic primordial dwarfism type II | PcntGt(RRU388)Byg/PcntGt(RRU388)Byg | B6.129P2-PcntGt(RRU388)Byg | J:226309 | 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 | ||||
multiple epiphyseal dysplasia 5 | Matn3tm1Mbri/Matn3tm1Mbri | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:125104 | View | ||||
osteogenesis imperfecta | Col1a1m1Btlr/Col1a1m1Btlr | C57BL/6J-Col1a1m1Btlr | J:253622 | View | ||||
osteogenesis imperfecta | Col1a2oim/Col1a2+ | B6C3Fe a/a-Col1a2oim/J | J:38013 | View | ||||
osteogenesis imperfecta | Col1a2tm1.1Mcbr/Col1a2+ | (A/J x B6.129-Col1a2tm1.1Mcbr)F1 | J:178743 | View | ||||
osteogenesis imperfecta | Col1a2tm1.1Mcbr/Col1a2+ | (BALB/cByJ x B6.129-Col1a2tm1.1Mcbr)F1 | J:178743 | View | ||||
osteogenesis imperfecta | Col1a2tm1.1Mcbr/Col1a2+ | (C3H/HeJ x B6.129-Col1a2tm1.1Mcbr)F1 | J:178743 | View | ||||
osteogenesis imperfecta | Col1a2tm1.1Mcbr/Col1a2+ | (FVB/NJ x B6.129-Col1a2tm1.1Mcbr)F1 | J:178743 | 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 | ||||
osteogenesis imperfecta type 6 | Serpinf1tm1Craw/Serpinf1tm1Craw | Not Specified | J:230409 | View | ||||
osteogenesis imperfecta type 7 | Crtaptm1Brle/Crtaptm1Brle | involves: 129S7/SvEvBrd | J:116096 | View | ||||
osteogenesis imperfecta type 8 | P3h1tm1Dgen/P3h1tm1Dgen | involves: C57BL/6 | J:163884 | View | ||||
osteogenesis imperfecta type 9 | PpibGt(RST139)Byg/PpibGt(RST139)Byg | involves: 129P2/OlaHsd * C57BL/6 | J:226318 | View | ||||
osteogenesis imperfecta type 9 | Ppibtm1.1Rjb/Ppibtm1.1Rjb | Not Specified | J:161748 | View | ||||
osteogenesis imperfecta type 10 |
Serpinh1tm2Kzn/Serpinh1tm2Kzn Tg(Col2a1-cre)1Bhr/0 |
involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J * SJL | J:197791 | View | ||||
otospondylomegaepiphyseal dysplasia, autosomal recessive | Col11a2tm1Mne/Col11a2tm1Mne | FVB.129-Col11a2tm1Mne | J:71948 | 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 | ||||
progressive pseudorheumatoid arthropathy of childhood | Ccn6tm1(cre)Mawa/Ccn6tm1(cre)Mawa | involves: 129S4/SvJae * C57BL/6 | J:201718 | View | ||||
progressive pseudorheumatoid arthropathy of childhood | Ccn6tm2Mawa/Ccn6tm2Mawa | 129S/SvEv-Ccn6tm2Mawa | J:94500 | View | ||||
progressive pseudorheumatoid arthropathy of childhood | Ccn6tm2Mawa/Ccn6tm2Mawa | involves: 129S/SvEv * C57BL/6 | J:201718 | 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 | ||||
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 | ||||
Schimke immuno-osseous dysplasia | Smarcal1tm1.1Cfbo/Smarcal1tm1.1Cfbo | either: B6.129-Smarcal1tm1.1Cfbo or (involves: 129 * C57BL/6) | J:183899 | View | ||||
Schmid metaphyseal chondrodysplasia | Col10a1tm1.1Rpbh/Col10a1tm1.1Rpbh | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:154052 | View | ||||
Schmid metaphyseal chondrodysplasia | Col10a1tm2.1Rpbh/Col10a1+ | involves: C57BL/6NTac | J:267200 | View | ||||
Schmid metaphyseal chondrodysplasia | Col10a1tm2.1Rpbh/Col10a1tm2.1Rpbh | involves: C57BL/6NTac | J:267200 | View | ||||
schneckenbecken dysplasia | Slc35d1tm1Hko/Slc35d1tm1Hko | involves: 129S1/Sv * 129X1/SvJ | J:130304 | View | ||||
short-rib thoracic dysplasia 7 with or without polydactyly | Wdr35yeti/Wdr35yeti | Not Specified | J:171617 | View | ||||
short-rib thoracic dysplasia 9 with or without polydactyly | Ift140b2b1283Clo/Ift140b2b1283Clo | C57BL/6J-Ift140b2b1283Clo | J:175213 | View | ||||
Silverman-Handmaker type dyssegmental dysplasia | Hspg2tm1Nid/Hspg2tm1Nid | involves: 129X1/SvJ * C57BL/6 | J:74542 | View | ||||
Silverman-Handmaker type dyssegmental dysplasia | Hspg2tm1Ref/Hspg2tm1Ref | involves: 129S1/Sv * 129X1/SvJ | J:84739 | View | ||||
Smith-McCort dysplasia 2 | Rab33bem1Rmr/Rab33b+ | involves: C57BL/6 | J:338833 | View | ||||
Smith-McCort dysplasia 2 | Rab33bem1Rmr/Rab33bem1Rmr | involves: C57BL/6 | J:338833 | 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 | ||||
spondylocarpotarsal synostosis syndrome | FlnbGt(RRF239)Byg/FlnbGt(RRF239)Byg | involves: 129P2/OlaHsd * C57BL/6 | J:132026 | View | ||||
spondylocarpotarsal synostosis syndrome | FlnbGt(XD076)Byg/FlnbGt(XD076)Byg | involves: 129P2/OlaHsd * C57BL/6 | J:134094 | View | ||||
spondyloepimetaphyseal dysplasia, Pakistani type | Papss2bm/Papss2bm | LDJ/Le | J:5109 | 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 | ||||
thanatophoric dysplasia | Fgfr3tm1Llm/Fgfr3+ | involves: 129S2/SvPas * C57BL/6J | J:147208 | View | ||||
thanatophoric dysplasia | Fgfr3tm4.1Cxd/Fgfr3+ | involves: 129S6/SvEvTac * NIH Black Swiss | J:63198 | View | ||||
thanatophoric dysplasia |
Fgfr3tm4Cxd/Fgfr3+ Tg(Col2a1-cre)1Bhr/0 |
involves: 129S6/SvEvTac * C57BL/6 * NIH Black Swiss * SJL | J:63198 | View | ||||
thanatophoric dysplasia | Fgfr3tm5.1Cxd/Fgfr3+ | involves: 129S6/SvEvTac | J:67780 | View | ||||
achondroplasia | Acancmd/Acancmd | involves: STOCK T tlow Itpr3tf | J:5952, J:30795 | View | ||||
achondroplasia | Nppclbab/Nppclbab | B6.PL-Nppclbab/GrsrJ | J:122924 | View | ||||
achondroplasia | Nppctm1Yog/Nppctm1Yog | either: 129X1/SvJ or (involves: 129 * C57BL/6J) | J:75620 | View | ||||
achondroplasia | Npr2cn-2J/Npr2cn-2J | B6;CBACa-Aw-J/A-Kcnj6wv/+ | J:72465 | View | ||||
achondroplasia | Npr2cn-3J/Npr2cn-3J | MRL/MpJ-Npr2cn-3J/GrsrJ | J:170669 | View | ||||
achondroplasia | Npr2cn/Npr2cn | involves: AKR/J | J:26341 | View | ||||
achondroplasia | Pthlhtm1Hmk/Pthlhtm1Hmk | either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6) | J:16911 | View | ||||
achondroplasia | Spred2Gt(XB228)Byg/Spred2Gt(XB228)Byg | involves: 129P2/OlaHsd * C57BL/6 | J:100826 | View | ||||
asphyxiating thoracic dystrophy | Smarcad1tm1Gos/Smarcad1tm1Gos | 129S2/SvPas-Smarcad1tm1Gos | J:208500 | View | ||||
asphyxiating thoracic dystrophy | srt/srt | Not Specified | J:75360 | View | ||||
asphyxiating thoracic dystrophy 1 | Ift140cauli/Ift140cauli | involves: C3H/HeH * C57BL/6JAnu | J:220659 | View | ||||
asphyxiating thoracic dystrophy 3 | Ift80Gt(AN0245)Wtsi/Ift80Gt(AN0245)Wtsi | involves: 129P2/OlaHsd | J:169236 | View | ||||
bone development disease | Tg(Col11a2-Npr2*)28Keoz/0 | involves: C57BL/6 | J:189658 | View | ||||
cleidocranial dysplasia | Ccd/Ccd+ | B10Rl.101-Ccd | J:16170 | View | ||||
cleidocranial dysplasia | Ccd/Ccd+ | involves: 101 * C3H | J:14006 | View | ||||
clubfoot | cl/cl | Not Specified | J:294 | View | ||||
clubfoot | Dbf/Dbf+ | involves: 101/H * C3H/HeH | J:39106 | View | ||||
clubfoot | Fkbp8tm1Kei/Fkbp8tm1Kei | involves: 129P2/OlaHsd * C57BL/6J | J:132961 | View | ||||
clubfoot | Fras1bl/Fras1bl | involves: 101/H * C3H/HeH | J:83745 | View | ||||
clubfoot | Grip1eb/Grip1eb | involves: hairless stock | J:13412 | View | ||||
clubfoot | pma/pma | involves: CF-1 | J:8195 | View | ||||
clubfoot |
Rettm1Kln/Rettm1Kln Tg(Nes-cre)1Kln/0 |
involves: 129/Sv * BALB/c * C57BL/6 * CBA/J * SJL | J:110955 | View | ||||
clubfoot | skc3/skc3 | involves: C57BL/6J | J:85113 | View | ||||
clubfoot | Tcirg1oc/Tcirg1oc | C57BL/6J-Vps33abf | J:28464 | View | ||||
clubfoot | vsd/vsd | C57BL/6J-vsd | J:94456 | View | ||||
craniosynostosis | Axin2tm1Wbm/Axin2tm1Wbm | involves: 129P2/OlaHsd * C57BL/6 | J:98523 | View | ||||
Crouzon syndrome | Bey/Bey+ | 129S/SvEv-Bey | J:47965 | View | ||||
dysostosis |
Kif3atm2Gsn/Kif3atm2Gsn H2az2Tg(Wnt1-cre)11Rth/H2az2+ |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J | J:158523 | View | ||||
hypertrichotic osteochondrodysplasia Cantu type | Kcnj8em1Nich/Kcnj8+ | involves: C57BL/6J * CBA/J | J:281903 | View | ||||
hypochondrogenesis | Tg(Col2a1*G574S)1Waho/0 | involves: C57BL/6 * DBA/2 | J:38204 | View | ||||
Leri-Weill dyschondrosteosis |
Shox2tm1Ddu/Shox2tm1.1Ddu Tg(Prrx1-cre)1Cjt/0 |
involves: 129S2/SvPas * C57BL/6J * SJL/J | J:107668 | View | ||||
multiple epiphyseal dysplasia | Comptm1Mbri/Comptm1Mbri | involves: 129S1/Sv * 129X1/SvJ | J:154984 | 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 | ||||
osteochondrodysplasia | Atf2tm1Glm/Atf2tm1Glm | involves: 129S2/SvPas | J:30611 | View | ||||
osteochondrodysplasia | Cebpbtm1Kish/Cebpbtm1Kish | involves: 129P2/OlaHsd | J:237461 | View | ||||
osteochondrodysplasia | Mir140em1Tkob/Mir140+ | C57BL/6-Mir140em1Tkob | J:286036 | View | ||||
osteochondrodysplasia | Mir140em1Tkob/Mir140em1Tkob | C57BL/6-Mir140em1Tkob | J:286036 | View | ||||
osteochondrodysplasia | Nppclbab/Nppclbab | B6.PL-Nppclbab/GrsrJ | J:321139 | View | ||||
osteochondrodysplasia |
Rnf146tm1.1Rtpl/Rnf146tm1.1Rtpl Tg(Sp7-tTA,tetO-EGFP/cre)1Amc/0 |
involves: C57BL/6J * CD-1 | J:244583 | View | ||||
osteogenesis imperfecta |
Smad4tm2.1Cxd/Smad4tm2.1Cxd Tg(Sp7-tTA,tetO-EGFP/cre)1Amc/0 |
involves: 129S6/SvEvTac * C57BL/6J * CD-1 | J:211171 | View | ||||
osteogenesis imperfecta | Smpd3fro/Smpd3fro | Not Specified | J:100158 | 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 | ||||
Smith-McCort dysplasia | DymGt(GTR1.3)1Rul/DymGt(GTR1.3)1Rul | involves: 129 | J:141099 | View | ||||
split hand-foot malformation | Map3k20em2Smun/Map3k20em2Smun | involves: 129S6/SvEvTac * C57BL/6NCrl | J:231477 | View | ||||
split hand-foot malformation 1 | Dlx5/Dlx6tm1Levi/Dlx5/Dlx6tm1Levi | Not Specified | J:77244 | View | ||||
spondylocostal dysostosis | Dll3tm1Rbe/Dll3tm1Rbe | involves: 129P2/Ola * C57BL/6 | J:75954 | View | ||||
spondylocostal dysostosis | Hes7M1Btlr/Hes7+ | C57BL/6J-Hes7M1Btlr | J:307652 | View | ||||
spondylocostal dysostosis | Ripply2tm1Asas/Ripply2tm1Asas | involves: C57BL/6 * CBA | J:122747 | View | ||||
spondyloepimetaphyseal dysplasia | Col2a1Rgsc413/Col2a1Rgsc413 | involves: C57BL/6JJcl * DBA/2JJcl | J:260538 | View | ||||
spondyloepimetaphyseal dysplasia | Col2a1Rgsc856/Col2a1Rgsc856 | involves: C57BL/6JJcl * DBA/2JJcl | J:171906 | View | ||||
spondyloepiphyseal dysplasia congenita | Hapln1tm1Nid/Hapln1tm1Nid | involves: 129S1/Sv * 129X1/SvJ | J:52575 | View | ||||
syndactyly | b2b1594Clo/b2b1594Clo | C57BL/6J-b2b1594Clo | J:175213 | View | ||||
synpolydactyly | Hoxd13spdh/Hoxd13spdh | B6C3Fe a/a-Hoxd13spdh/J | J:47974 | View | ||||
synpolydactyly | Hoxd13tm1Ddu/Hoxd13tm1Ddu | either: (involves: 129S2/SvPas * 129/Sv) or (involves: 129S2/SvPas * C57BL/6) | J:15507 | View | ||||
synpolydactyly | Hoxd13tm1Mrc/Hoxd13tm1Mrc | involves: 129S7/SvEvBrd | J:32603 | View | ||||
thanatophoric dysplasia | Hspg2tm1Nid/Hspg2tm1Nid | involves: 129X1/SvJ * C57BL/6 | J:67299 | View | ||||
Weissenbacher-Zweymuller syndrome | Acvr2atm1Zuk/Acvr2atm1Zuk | either: 129 or (involves: 129S7/SvEvBrd * C57BL/6) | J:23924 | View | ||||
Weissenbacher-Zweymuller syndrome | hpmd/hpmd | Not Specified | J:75360 | View | ||||
Weissenbacher-Zweymuller syndrome |
Mapk1tm1Gela/Mapk1tm1Gela H2az2Tg(Wnt1-cre)11Rth/H2az2+ |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6J * CBA/J | J:239772 | View | ||||
Weissenbacher-Zweymuller syndrome |
Sox11tm1.1Gan/Sox11tm1.1Gan Tg(EIIa-cre)C5379Lmgd/0 |
involves: 129S6/SvEvTac * C57BL/6 * FVB/N | J:232434 | View | ||||
Weissenbacher-Zweymuller syndrome |
Tfrctm3.1Nca/Tfrctm3.1Nca H2az2Tg(Wnt1-cre)11Rth/H2az2+ |
involves: 129S4/SvJae * C57BL/6J * CBA/J | J:316198 | View | ||||
Transgenes and Other Mutations | achondroplasia | Tg(FGFR3-G380R)7Aya/0 | involves: BALB/c * C57BL/6 | J:59887 | View | |||
achondroplasia | Tg(FGFR3-G380R)7Aya/Tg(FGFR3-G380R)7Aya | involves: BALB/c * C57BL/6 | J:59887 | View | ||||
craniosynostosis | Tg(Nell1)1Ting/0 | involves: C3H * C57BL/6 | J:79106 | View | ||||
osteogenesis imperfecta type 1 | Tg(COL1A1)73Prc/0 | involves: FVB/N | J:146429 | View | ||||
pseudoachondroplasia | Tg(Col2a1-rtTA,tetO-COMP*)2Jath/0 | C57BL/6-Tg(Col2a1-rtTA,tetO-COMP*)2Jath | J:152756, J:233238 | View | ||||
Additional Complex Models | acrocephalosyndactylia |
Spry2tm1Ayos/Spry2tm1Ayos Spry4tm1Ayos/Spry4tm1Ayos |
involves: 129 * C57BL/6J | J:116506 | View | |||
brachydactyly type A1 | ShhDsh/Shh+ | B10Rl.Cg-ShhDsh | J:97323 | View | ||||
osteogenesis imperfecta |
Bmp1tm1.1Dgr/Bmp1tm1.1Dgr Tll1tm2.1Dgr/Tll1tm2.1Dgr Ndor1Tg(UBC-cre/ERT2)1Ejb/0 |
involves: 129S/SvEv * 129S6/SvEvTac * C57BL/6 * SJL | J:210366 | View | ||||
split hand-foot malformation 3 |
Fbxw4Dac-2J/Fbxw4+ mdac/mdac |
CBy.MRL-Fbxw4Dac-2J/J | J:133888 | View | ||||
split hand-foot malformation 3 |
Fbxw4Dac/Fbxw4+ mdac/mdac |
involves: SM/Ckc | J:29220, J:133888 | View | ||||
spondylocostal dysostosis | Tbx6rv/Tbx6rv | involves: C57BL/J * C57BL/6J | J:8119 | 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 | ||||
Weissenbacher-Zweymuller syndrome |
Ptprftm1Wjh/Ptprftm1Wjh Ptprstm1Mtr/Ptprstm1Mtr |
B6.Cg-Ptprftm1Wjh Ptprstm1Mtr | J:199299 | 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 | achondroplasia | Fgfr3tm1Dor/Fgfr3tm1Dor | involves: 129S6/SvEvTac * C57BL/6 | J:32991 | View | |||
brachydactyly type B1 | Ror2tm1Anec/Ror2+ | B6.129S1-Ror2tm1Anec | J:134490 | View | ||||
multiple epiphyseal dysplasia | Comptm1Aol/Comptm1Aol | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:76781 | View | ||||
osteogenesis imperfecta type 5 | Ifitm5em1Pmof/Ifitm5+ | involves: CD-1 | J:255349 | View | ||||
pseudoachondroplasia | Comptm1Aol/Comptm1Aol | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:76781 | View | ||||
thanatophoric dysplasia | Fgfr3tm1Cxd/Fgfr3tm1Cxd | involves: 129S6/SvEvTac * NIH Black Swiss | J:52438 | View |