|
Symbol Name ID |
Arhgap31
Rho GTPase activating protein 31 MGI:1333857 |
| Darker colors indicate more annotations |
| Human Phenotypes | Microcephaly |
Encephalocele |
Lateral ventricle dilatation |
Hydrocephalus |
Ventriculomegaly |
Pachygyria |
Polymicrogyria |
Cortical dysplasia |
Hypoplasia of the corpus callosum |
Periventricular leukomalacia |
Cerebral atrophy |
Porencephalic cyst |
Cerebellar hypoplasia |
Retrocerebellar cyst |
Hemiparesis |
EEG abnormality |
Delayed speech and language development |
Intellectual disability |
Intellectual disability, mild |
Global developmental delay |
Severe global developmental delay |
Delayed gross motor development |
Seizure |
| Disease(s) Associated with ARHGAP31 | |||||||||||||||||||||||
| Adams-Oliver syndrome |
| Mouse Phenotypes | abnormal brain meninges morphology |
decreased prepulse inhibition |
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| Availability | Mouse Genotype | ||
| Arhgap31tm1.2Itl/Arhgap31tm1.2Itl | |||
| Arhgap31em1(IMPC)Bay/Arhgap31+ | |||
| Arhgap31tm1.1Itl/Arhgap31tm1.2Itl | |||
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 04/30/2024 MGI 6.23 |
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