|
Symbol Name ID |
Kif14
kinesin family member 14 MGI:1098226 |
| Darker colors indicate more annotations |
| Human Phenotypes | Micrognathia |
Dandy-Walker malformation |
Microcephaly |
Encephalocele |
Full cheeks |
Sloping forehead |
Thin upper lip vermilion |
Cleft palate |
Aplasia/Hypoplasia of the tongue |
Furrowed tongue |
Depressed nasal ridge |
Upslanted palpebral fissure |
| Disease(s) Associated with KIF14 | ||||||||||||
| Meckel syndrome | ||||||||||||
| primary autosomal recessive microcephaly |
| Mouse Phenotypes | flat head |
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| Availability | Mouse Genotype | |
| Kif14tm1Tskk/Kif14tm1Tskk | ||
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 04/30/2024 MGI 6.23 |
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