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Symbol
Name
ID

Rab23
RAB23, member RAS oncogene family
MGI:99833

Phenotype annotations related to nervous system

!	Indicates phenotype varies with strain background.
	Darker colors indicate more annotations

Human Phenotypes	Aplasia/Hypoplasia of the corpus callosum	Cerebral atrophy	Spina bifida occulta	Intellectual disability	Global developmental delay	Delayed ability to walk	Generalized non-motor (absence) seizure
Disease(s) Associated with RAB23
Carpenter syndrome

Mouse Phenotypes

abnormal neural tube morphology

abnormal neural tube closure

incomplete caudal neuropore closure

open neural tube

spina bifida

spina bifida occulta

abnormal neural tube ventricular layer morphology

abnormal postnatal subventricular zone morphology

exencephaly

abnormal dorsal root ganglion morphology

abnormal spinal cord morphology

abnormal spinal cord central canal morphology

Availability

Mouse Genotype

Rab23^opb2/Rab23^opb2

Rab23^opb/Rab23^opb

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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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