Symbol Name ID |
Kif7
kinesin family member 7 MGI:1098239 |
Darker colors indicate more annotations |
Human Phenotypes | Hydrocephalus |
Ventriculomegaly |
Aplasia/Hypoplasia of the corpus callosum |
Agenesis of corpus callosum |
Anencephaly |
Molar tooth sign on MRI |
Intracranial cystic lesion |
Intellectual disability |
Intellectual disability, severe |
Seizure |
Disease(s) Associated with KIF7 | ||||||||||
acrocallosal syndrome | ||||||||||
hydrolethalus syndrome 2 |
Mouse Phenotypes | abnormal neuron differentiation |
abnormal neural tube morphology |
hydrocephaly |
exencephaly |
abnormal motor neuron morphology |
increased motor neuron number |
abnormal spinal cord morphology |
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Availability | Mouse Genotype | |||||||
Kif7b2b2254Clo/Kif7b2b2254Clo | ||||||||
Kif7dda/Kif7dda | ||||||||
Kif7maki/Kif7maki Tg(Hlxb9-GFP)1Tmj/? |
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Kif7tm1.2Hui/Kif7tm1.2Hui | ||||||||
Kif7tm1Lex/Kif7tm1Lex |
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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