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Symbol
Name
ID
Kif7
kinesin family member 7
MGI:1098239
Phenotype annotations related to nervous system
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
Availability Mouse Genotype
Kif7b2b2254Clo/Kif7b2b2254Clo
Kif7dda/Kif7dda
Kif7maki/Kif7maki
Tg(Hlxb9-GFP)1Tmj/?
Kif7tm1.2Hui/Kif7tm1.2Hui
Kif7tm1Lex/Kif7tm1Lex

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
04/23/2024
MGI 6.23
The Jackson Laboratory