Excel File Text File All mouse models of congenital hemolytic anemia with phenotypic similarity to the human disease
        Disease Term Allelic Composition Genetic Background Reference Phenotypes
      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
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
      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
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


       
No similarity to the expected human disease phenotype was found.
        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