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Symbol
Name
ID

Rdh12
retinol dehydrogenase 12
MGI:1925224

Phenotype annotations related to vision/eye

Darker colors indicate more annotations

Human Phenotypes	Central retinal vessel vascular tortuosity	Attenuation of retinal blood vessels	Optic atrophy	Optic disc pallor	Leber optic atrophy	Optic neuropathy	Bone spicule pigmentation of the retina	Retinal dystrophy	Reduced visual acuity	Centrocecal scotoma	Visual loss
Disease(s) Associated with RDH12	Central retinal vessel vascular tortuosity	Attenuation of retinal blood vessels	Optic atrophy	Optic disc pallor	Leber optic atrophy	Optic neuropathy	Bone spicule pigmentation of the retina	Retinal dystrophy	Reduced visual acuity	Centrocecal scotoma	Visual loss
Leber congenital amaurosis 13
Leber hereditary optic neuropathy

Mouse Phenotypes		abnormal retina apoptosis	short retina rod cell outer segment	abnormal retina neuronal layer morphology	abnormal eye physiology	abnormal eye electrophysiology	delayed dark adaptation
Availability	Mouse Genotype	abnormal retina apoptosis	short retina rod cell outer segment	abnormal retina neuronal layer morphology	abnormal eye physiology	abnormal eye electrophysiology	delayed dark adaptation
	Rdh12^tm1.1Cahb/Rdh12^tm1.1Cahb
	Rdh12^tm1Kpal/Rdh12^tm1Kpal
	Rdh12^tm1Kpal/Rdh12⁺

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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 04/23/2024 MGI 6.23