Entity Details

Primary name RDH11_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ8TC12
EntryNameRDH11_HUMAN
FullNameRetinol dehydrogenase 11
TaxID9606
Evidenceevidence at protein level
Length318
SequenceStatuscomplete
DateCreated2003-08-29
DateModified2021-06-02

Ontological Relatives

GenesRDH11

GO terms

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GOName
GO:0001523 retinoid metabolic process
GO:0004745 NAD-retinol dehydrogenase activity
GO:0005789 endoplasmic reticulum membrane
GO:0016021 integral component of membrane
GO:0042572 retinol metabolic process
GO:0042574 retinal metabolic process
GO:0052650 NADP-retinol dehydrogenase activity
GO:0102354 11-cis-retinol dehydrogenase activity
GO:0110095 cellular detoxification of aldehyde

Subcellular Location

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Subcellular Location
Endoplasmic reticulum membrane

Domains

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DomainNameCategoryType
IPR002347 Short-chain dehydrogenase/reductase SDRFamilyFamily
IPR036291 NAD(P)-binding domain superfamilyFamilyHomologous superfamily

Diseases

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Disease IDSourceNameDescription
616108 OMIMRetinal dystrophy, juvenile cataracts, and short stature syndrome (RDJCSS)A disorder characterized by retinal dystrophy resulting in progressive decrease in visual acuity and difficulties with night vision in the first decade of life, development of juvenile cataracts, facial dysmorphism, psychomotor developmental delays, learning disabilities and short stature. Ophthalmological findings include salt-and-pepper retinopathy, attenuation of the arterioles, generalized rod-cone dysfunction, mottled macula at an early age, and peripapillary sparing of the retinal pigment epithelium. The disease is caused by variants affecting the gene represented in this entry.

Drugs

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DrugNameSourceType
DB00162 Vitamin ADrugbanksmall molecule