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Symbol Name ID |
Kif26a
kinesin family member 26A MGI:2447072 |
| Darker colors indicate more annotations |
| Human Phenotypes | Colpocephaly |
Hydrocephalus |
Ventriculomegaly |
Polymicrogyria |
Agenesis of corpus callosum |
Hypoplasia of the corpus callosum |
Reduced cerebral white matter volume |
Cerebral atrophy |
Schizencephaly |
Global developmental delay |
Seizure |
| Disease(s) Associated with KIF26A | |||||||||||
| complex cortical dysplasia with other brain malformations 11 |
| Mouse Phenotypes | abnormal axon extension |
abnormal neuronal precursor proliferation |
abnormal enteric ganglia morphology |
abnormal enteric neuron morphology |
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| Availability | Mouse Genotype | ||||
| Kif26atm1.1Noh/Kif26atm1.1Noh | |||||
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 03/24/2026 MGI 6.24 |
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