|
Symbol Name ID |
Kif2a
kinesin family member 2A MGI:108390 |
| Darker colors indicate more annotations |
| Human Phenotypes | Microcephaly |
Spastic tetraplegia |
Lissencephaly |
Agyria |
Pachygyria |
Subcortical band heterotopia |
Cortical dysplasia |
Thin corpus callosum |
Hypoplasia of the corpus callosum |
Gray matter heterotopia |
Global developmental delay |
Seizure |
| Disease(s) Associated with KIF2A | ||||||||||||
| complex cortical dysplasia with other brain malformations 3 |
| Mouse Phenotypes | abnormal axon extension |
abnormal neuronal migration |
enlarged brain ventricles |
abnormal inferior olivary complex morphology |
abnormal midbrain morphology |
abnormal tegmentum morphology |
abnormal trigeminal V mesencephalic nucleus morphology |
abnormal pons morphology |
abnormal pontine nuclei morphology |
abnormal forebrain morphology |
abnormal hippocampus layer morphology |
abnormal stratification in cerebral cortex |
abnormal hindbrain morphology |
abnormal cerebellum morphology |
abnormal nervous system development |
abnormal axon morphology |
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| Availability | Mouse Genotype | ||||||||||||||||
| Kif2atm1Noh/Kif2atm1Noh | |||||||||||||||||
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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