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Symbol
Name
ID

Rab18
RAB18, member RAS oncogene family
MGI:102790

Phenotype annotations related to vision/eye

Darker colors indicate more annotations

Human Phenotypes	Shallow anterior chamber	Microcornea	Cataract	Developmental cataract	Optic atrophy	Microphthalmia	Miosis	Nystagmus	Cerebral visual impairment
Disease(s) Associated with RAB18
Warburg micro syndrome 3

Mouse Phenotypes		abnormal pupillary reflex	optic nerve degeneration	abnormal pupil morphology	miotic pupil	nuclear cataract	abnormal eye development	microphthalmia
Availability	Mouse Genotype	abnormal pupillary reflex	optic nerve degeneration	abnormal pupil morphology	miotic pupil	nuclear cataract	abnormal eye development	microphthalmia
	Rab18^{Gt(EUCE0233a03)Hmgu}/Rab18^{Gt(EUCE0233a03)Hmgu}
	Rab18^m1Hongc/Rab18^m1Hongc

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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