|
Symbol Name ID |
Kif7
kinesin family member 7 MGI:1098239 |
| Darker colors indicate more annotations |
| Human Phenotypes | Optic atrophy |
Hypopigmentation of the fundus |
Hypertelorism |
Coloboma |
Strabismus |
Nystagmus |
| Disease(s) Associated with KIF7 | ||||||
| acrocallosal syndrome |
| Mouse Phenotypes | microphthalmia |
anophthalmia |
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| Availability | Mouse Genotype | ||
| Kif7b2b2254Clo/Kif7b2b2254Clo | |||
| Kif7tm1Lex/Kif7tm1Lex | |||
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 04/23/2024 MGI 6.23 |
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