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Symbol
Name
ID
Kif14
kinesin family member 14
MGI:1098226
Phenotype annotations related to vision/eye
Darker colors indicate more annotations
Human Phenotypes
Microcornea
Sclerocornea
Cataract
Aplasia/Hypoplasia of the iris
Abnormal chorioretinal morphology
Optic atrophy
Hypertelorism
Anophthalmia
Microphthalmia
Disease(s) Associated with KIF14
Meckel syndrome

Mouse Phenotypes
optic nerve hypoplasia
Availability Mouse Genotype
Kif14tm1Tskk/Kif14tm1Tskk

Contributing Projects:
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
The Jackson Laboratory