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Symbol Name ID |
Kif5a
kinesin family member 5A MGI:109564 |
| Darker colors indicate more annotations |
| Human Phenotypes | Rod-cone dystrophy |
| Disease(s) Associated with KIF5A | |
| hereditary spastic paraplegia 10 |
| Mouse Phenotypes | impaired pupillary reflex |
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| Availability | Mouse Genotype | |
| Kif5atm1b(EUCOMM)Wtsi/Kif5a+ | ||
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 04/16/2024 MGI 6.23 |
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