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Symbol
Name
ID
Rab23
RAB23, member RAS oncogene family
MGI:99833
Phenotype annotations related to vision/eye
Darker colors indicate more annotations
Human Phenotypes
Abnormal cornea morphology
Opacification of the corneal stroma
Microcornea
Optic atrophy
Blue sclerae
Hypertelorism
Disease(s) Associated with RAB23
Carpenter syndrome

Mouse Phenotypes
abnormal eye morphology
abnormal lens induction
abnormal lens vesicle development
abnormal optic cup morphology
abnormal retina neuronal layer morphology
anophthalmia
Availability Mouse Genotype
Rab23opb2/Rab23opb2
Rab23opb/Rab23opb

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
04/16/2024
MGI 6.23
The Jackson Laboratory