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All mouse models of normocytic anemia with phenotypic similarity to the human disease
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Disease Term | Allelic Composition | Genetic Background | Reference | Phenotypes | ||||
aplastic anemia | Ifngtm1.1Hayg/Ifngtm1.1Hayg | Not Specified | J:220784 | View | ||||
congenital nonspherocytic hemolytic anemia | Gpi1b-m1Neu/Gpi1b-m1Neu | C3.Cg-Gpi1b-m1Neu | J:35956 | View | ||||
congenital nonspherocytic hemolytic anemia | Gpi1b-m2Neu/Gpi1b-m2Neu | C3.Cg-Gpi1b-m2Neu | J:35956 | 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 | ||||
Fanconi anemia complementation group A | Fancatm1.1Wong/Fancatm1.1Wong | involves: C57BL/6 | J:85108 | View | ||||
Fanconi anemia complementation group A | Fancatm1Faw/Fancatm1Faw | involves: 129P2/OlaHsd * FVB | J:63742 | View | ||||
Fanconi anemia complementation group A | Fancatm1Wong/Fancatm1Wong | involves: C57BL/6 | J:85108 | View | ||||
Fanconi anemia complementation group C | Fancctm1Mab/Fancctm1Mab | involves: 129S1/Sv * 129X1/SvJ * C57BL/6J | J:32080 | View | ||||
Fanconi anemia complementation group C | Fancctm1Mgo/Fancctm1Mgo | involves: 129S4/SvJaeSor * C57BL/6 | J:61512 | View | ||||
Fanconi anemia complementation group D1 | Brca2tm1Kamc/Brca2tm1Kamc | involves: 129P2/OlaHsd * BALB/c | J:144998 | View | ||||
Fanconi anemia complementation group D2 |
Aldh2tm1a(EUCOMM)Wtsi/Aldh2tm1a(EUCOMM)Wtsi Fancd2tm1Hou/Fancd2tm1Hou |
involves: 129S4/SvJae * C57BL/6J * C57BL/6N | J:193232 | View | ||||
Fanconi anemia complementation group D2 | Fancd2em1Tzh/Fancd2em1Tzh | C57BL/6-Fancd2em1Tzh | J:284566 | View | ||||
Fanconi anemia complementation group D2 |
Fancd2Gt(OST57859)Lex/Fancd2Gt(OST57859)Lex Usp1tm1.1Ada/Usp1tm1.1Ada |
involves: 129S5/SvEvBrd * C57BL/6 | J:146616 | View | ||||
Fanconi anemia complementation group D2 | Fancd2tm1Hou/Fancd2tm1Hou | 129S4/SvJae-Fancd2tm1Hou | J:84892 | View | ||||
Fanconi anemia complementation group D2 | Fancd2tm1Hou/Fancd2tm1Hou | B6.129S4-Fancd2tm1Hou | J:84892 | View | ||||
Fanconi anemia complementation group D2 | Fancd2tm1Hou/Fancd2tm1Hou | involves: 129S4/SvJae * C57BL/6J | J:84892 | 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 | ||||
hereditary spherocytosis type 3 | Spta1ihj/Spta1ihj | involves: HRS/J * LAH | J:157766 | View | ||||
hereditary spherocytosis type 3 | Spta1sph-2Bc/Spta1sph-2Bc | involves: SELH | J:7048, J:7501 | View | ||||
hereditary spherocytosis type 3 | Spta1sph-ha/Spta1sph-ha | involves: DBA/1J | J:14946, J:30699 | View | ||||
hereditary spherocytosis type 3 | Spta1sph/Spta1sph | either: (B6.C3-Spta1sph x WB.C3-Spta1sph)F1 or (WB.C3-Spta1sph x B6.C3-Spta1sph)F1 | J:6695 | View | ||||
hereditary spherocytosis type 3 | Spta1sph/Spta1sph | involves: C3H | J:12276 | View | ||||
pyruvate kinase deficiency of red cells | Pklrchar4/Pklrchar4 | involves: A/J * C57BL/6 | J:86735 | View | ||||
pyruvate kinase deficiency of red cells | Pklrslc/Pklrslc | CBA/NSlc-Pklrslc | J:29199 | View | ||||
aplastic anemia | Rasa3scat/Rasa3scat | involves: BALB/cBy * BALB/cByJ | J:281271 | View | ||||
autoimmune hemolytic anemia |
Tg(KRT5-rtTA)1Glk/0 Tg(tetO/CMV-Tslp)#Sfz/0 |
C.Cg-Tg(KRT5-rtTA)1Glk Tg(tetO/CMV-Tslp)#Sfz | J:182756 | View | ||||
congenital dyserythropoietic anemia |
Diaph3tm1.1Pji/Diaph3tm1.1Pji Tg(Mx1-cre)1Cgn/0 |
involves: C57BL/6J * CBA/J | J:293763 | View | ||||
congenital dyserythropoietic anemia | Man2a1tm1Jxm/Man2a1tm1Jxm | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:41621 | View | ||||
Diamond-Blackfan anemia | Flvcr1tm1.1Jlab/Flvcr1tm1.1Jlab | involves: 129S4/SvJae * C57BL/6 * DBA/2 | J:132057 | View | ||||
Diamond-Blackfan anemia |
Flvcr1tm1Jlab/Flvcr1tm1Jlab Tg(Mx1-cre)1Cgn/0 |
involves: 129S4/SvJae * C57BL/6 * CBA | J:132057 | View | ||||
Diamond-Blackfan anemia | Rpsatm1Ells/Rpsa+ | involves: 129S6/SvEvTac * C57BL/6 | J:138267 | View | ||||
Fanconi anemia | Usp1tm1.1Ada/Usp1tm1.1Ada | C57BL/6-Usp1tm1.1Ada | J:146616 | View | ||||
hereditary spherocytosis | Klf1Nan/Klf1+ | either: B6.Cg-Klf1Nan or WB.Cg-Klf1Nan | J:162530 | 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 | ||||
Diamond-Blackfan anemia |
Col1a1tm1(tetO-RNAi:Rps19)Karl/Col1a1+ Gt(ROSA)26Sortm1(rtTA*M2)Jae/Gt(ROSA)26Sortm1(rtTA*M2)Jae |
involves: 129S4/SvJae * C57BL/6 | J:179085 | View | ||||
Diamond-Blackfan anemia |
Col1a1tm1(tetO-RNAi:Rps19)Karl/Col1a1tm1(tetO-RNAi:Rps19)Karl Gt(ROSA)26Sortm1(rtTA*M2)Jae/Gt(ROSA)26Sortm1(rtTA*M2)Jae |
involves: 129S4/SvJae * C57BL/6 | J:179085 | View | ||||
Diamond-Blackfan anemia |
Col1a1tm2(tetO-RNAi:Rps19)Karl/Col1a1+ Gt(ROSA)26Sortm1(rtTA*M2)Jae/Gt(ROSA)26Sortm1(rtTA*M2)Jae |
involves: 129S4/SvJae * C57BL/6 | J:179085 | View | ||||
Diamond-Blackfan anemia |
Col1a1tm2(tetO-RNAi:Rps19)Karl/Col1a1tm2(tetO-RNAi:Rps19)Karl Gt(ROSA)26Sortm1(rtTA*M2)Jae/Gt(ROSA)26Sortm1(rtTA*M2)Jae |
involves: 129S4/SvJae * C57BL/6 | J:179085 | View | ||||
Transgenes and Other Mutations | Diamond-Blackfan anemia |
Tg(CAG-RPS19*R62W)#Dmb/0 Tg(Prnp-GFP/cre)1Blw/0 |
involves: 129S6/SvEvTac * FVB/N | J:165876 | View | |||
Additional Complex Models | autoimmune hemolytic anemia |
Tg(SV40-Igh-64C8)H3Hon/0 Tg(SV40-Igk4C8)L1Hon/0 |
involves: C57BL/6 | J:139864 | 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 | congenital dyserythropoietic anemia type III | Kif23tm1.1Igo/Kif23+ | involves: C57BL/6 * C57BL/6NTac | J:321429 | View | |||
congenital dyserythropoietic anemia type III | Kif23tm1.1Igo/Kif23tm1.1Igo | involves: C57BL/6 * C57BL/6NTac | J:321429 | View | ||||
Fanconi anemia complementation group P | Slx4tm1.2Jrou/Slx4tm1.2Jrou | B6.129P2-Slx4tm1.2Jrou | J:204996 | View | ||||
Rh deficiency syndrome | Rhagtm1Goo/Rhagtm1Goo | involves: 129P2/OlaHsd * C57BL/6 | J:182122 | View | ||||
Rh deficiency syndrome |
Rhagtm1Goo/Rhagtm1Goo Rhdtm1Goo/Rhdtm1Goo |
involves: 129P2/OlaHsd * C57BL/6 | J:182122 | View |