|
Symbol Name ID |
Kif5c
kinesin family member 5C MGI:1098269 |
| Darker colors indicate more annotations |
| Human Phenotypes | Microcephaly |
Secondary microcephaly |
Spastic tetraplegia |
Polymicrogyria |
Cortical dysplasia |
Hypoplasia of the corpus callosum |
EEG abnormality |
Absent speech |
Delusion |
Schizophrenia |
Hallucinations |
Negativism |
Motor stereotypy |
Self-injurious behavior |
Social and occupational deterioration |
Intellectual disability, severe |
Global developmental delay |
Seizure |
Clonic seizure |
| Disease(s) Associated with KIF5C | |||||||||||||||||||
| complex cortical dysplasia with other brain malformations 2 | |||||||||||||||||||
| schizophrenia |
| Mouse Phenotypes | decreased brain size |
decreased motor neuron number |
increased sensory neuron number |
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| Availability | Mouse Genotype | |||
| Kif5ctm1Noh/Kif5ctm1Noh | ||||
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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