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Symbol
Name
ID
Kif14
kinesin family member 14
MGI:1098226
Phenotype annotations related to skeleton
Darker colors indicate more annotations
Human Phenotypes
Micrognathia
Dandy-Walker malformation
Microcephaly
Encephalocele
Bowing of the long bones
Postaxial hand polydactyly
Preaxial hand polydactyly
Postaxial foot polydactyly
Abnormal cortical bone morphology
Disease(s) Associated with KIF14
Meckel syndrome
primary autosomal recessive microcephaly


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
04/30/2024
MGI 6.23
The Jackson Laboratory