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Symbol
Name
ID

Arhgap31
Rho GTPase activating protein 31
MGI:1333857

Phenotype annotations related to nervous system

Darker colors indicate more annotations

Human Phenotypes	Encephalocele	Hydrocephalus	Periventricular leukomalacia	Porencephalic cyst	Hemiparesis	EEG abnormality	Intellectual disability	Seizure
Disease(s) Associated with ARHGAP31
Adams-Oliver syndrome

Mouse Phenotypes		abnormal brain meninges morphology	decreased prepulse inhibition
Availability	Mouse Genotype	abnormal brain meninges morphology	decreased prepulse inhibition
	Arhgap31^tm1.2Itl/Arhgap31^tm1.2Itl
	Arhgap31^em1(IMPC)Bay/Arhgap31⁺
	Arhgap31^tm1.1Itl/Arhgap31^tm1.2Itl

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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