|
Symbol Name ID |
Kif14
kinesin family member 14 MGI:1098226 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Dandy-Walker malformation |
Microcephaly |
Encephalocele |
Hydrocephalus |
Ventriculomegaly |
Pachygyria |
Hypoplasia of the frontal lobes |
Aplasia/Hypoplasia of the corpus callosum |
Agenesis of corpus callosum |
Anencephaly |
Lobar holoprosencephaly |
Gray matter heterotopia |
Intellectual disability, severe |
Hyperreflexia |
Global developmental delay |
| Disease(s) Associated with KIF14 | |||||||||||||||
| Meckel syndrome | |||||||||||||||
| primary autosomal recessive microcephaly |
| Mouse Phenotypes | nervous system phenotype |
abnormal cerebellar granule cell migration |
decreased brain weight |
decreased brain size |
abnormal hippocampus morphology |
abnormal cerebral cortex morphology |
ectopic cerebral cortex pyramidal cells |
thin cerebral cortex |
abnormal olfactory bulb morphology |
small olfactory bulb |
abnormal cerebellar cortex morphology |
abnormal Purkinje cell dendrite morphology |
ectopic Purkinje cell |
cerebellum hypoplasia |
optic nerve hypoplasia |
abnormal spinal cord morphology |
abnormal oligodendrocyte physiology |
demyelination |
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| Availability | Mouse Genotype | ||||||||||||||||||
| Kif14lag/Kif14lag Tg(CAG-Kif14)28LTskk/0 |
* | ||||||||||||||||||
| Kif14lag/Kif14lag | |||||||||||||||||||
| 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 04/23/2024 MGI 6.23 |
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