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All mouse models of cytochrome-c oxidase deficiency disease with phenotypic similarity to the human disease
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| Disease Term | Allelic Composition | Genetic Background | Reference | Phenotypes | ||||
  | cytochrome-c oxidase deficiency disease |
Sco1tm1c(KOMP)Wtsi/Sco1tm1c(KOMP)Wtsi Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+ |
involves: C57BL/6 * C57BL/6N * DBA | J:222036 | View | |||
| cytochrome-c oxidase deficiency disease | Sco2tm1.1Easc/Sco2tm2.1Easc | 129X1/SvJ-Sco2tm1.1Easc/Sco2tm2.1Easc | J:155116 | View | ||||
| Leigh disease | Ndufs4tm1.1Rpa/Ndufs4tm1.1Rpa | B6.129S4-Ndufs4tm1.1Rpa | J:190475 | View | ||||
| Leigh disease |
Ndufs4tm1Rpa/Ndufs4tm1Rpa Tg(Nes-cre)1Kln/0 |
B6.Cg-Tg(Nes-cre)1Kln Ndufs4tm1Rpa | J:190475 | View | ||||
| Leigh disease |
Ndufs4tm1Rpa/Ndufs4tm1Rpa Tg(Nes-cre)1Kln/0 |
involves: 129S4/SvJaeSor * C57BL/6 * SJL | J:161393 | View | ||||
| Leigh disease | Surf1tm1Zev/Surf1tm1Zev | involves: 129S7/SvEvBrd * C57BL/6J * DBA/2 | J:81773 | View | ||||
| | cytochrome-c oxidase deficiency disease |
Cox10tm1Ctm/Cox10tm1Ctm Tg(Camk2a-cre)#Szi/0 |
involves: 129X1/SvJ * C57BL/6 * C57BL/6J * CBA | J:188773 | View | |||
| Leigh disease | Parltm1.1Bdes/Parltm1.1Bdes | involves: 129P2/OlaHsd | J:269785 | View | ||||
| Leigh disease |
Parltm1Bdes/Parltm1Bdes Tg(Nes-cre)1Kln/0 |
involves: 129P2/OlaHsd * C57BL/6 * SJL | J:269785 | View | ||||
| Leigh disease |
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 | ||||
| Leigh disease | Sod2tm1Cje/Sod2tm1Cje | involves: C57BL/6J | J:45913 | View | ||||