Mus musculus Gene: Rdh12
Summary
InnateDB Gene IDBG-152851.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol Rdh12
Gene Name retinol dehydrogenase 12
Synonyms A930033N07Rik
Species Mus musculus
Ensembl Gene ENSMUSG00000021123
Encoded Proteins
retinol dehydrogenase 12
retinol dehydrogenase 12
retinol dehydrogenase 12
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000139988:
The protein encoded by this gene is an NADPH-dependent retinal reductase whose highest activity is toward 9-cis and all-trans-retinol. The encoded enzyme also plays a role in the metabolism of short-chain aldehydes but does not exhibit steroid dehydrogenase activity. Defects in this gene are a cause of Leber congenital amaurosis type 3 (LCA3). [provided by RefSeq, Jul 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 12:79208914-79222665
Strand Forward strand
Band C3
Transcripts
ENSMUST00000021548 ENSMUSP00000021548
ENSMUST00000122227 ENSMUSP00000112543
ENSMUST00000151980
ENSMUST00000140823 ENSMUSP00000118851
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 4 interaction(s) predicted by orthology.
Predicted by orthology
Total 4 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0003824 catalytic activity
GO:0004745 retinol dehydrogenase activity
GO:0005515 protein binding
GO:0016491 oxidoreductase activity
GO:0050662 coenzyme binding
Biological Process
GO:0007601 visual perception
GO:0008152 metabolic process
GO:0042572 retinol metabolic process
GO:0044237 cellular metabolic process
GO:0050896 response to stimulus
GO:0055114 oxidation-reduction process
Cellular Component
GO:0005622 intracellular
Orthologs
Species
Homo sapiens
Bos taurus
Gene ID
Gene Order
Not yet available
Pathways
NETPATH
REACTOME
Disease pathway
The canonical retinoid cycle in rods (twilight vision) pathway
Visual phototransduction pathway
Signal Transduction pathway
Diseases associated with visual transduction pathway
KEGG
Retinol metabolism pathway
INOH
PID NCI
Pathway Predictions based on Human Orthology Data
NETPATH
REACTOME
The canonical retinoid cycle in rods (twilight vision) pathway
Signal Transduction pathway
Diseases associated with visual transduction pathway
Visual phototransduction pathway
Disease pathway
KEGG
Retinol metabolism pathway
INOH
PID NCI
Visual signal transduction: Cones
Visual signal transduction: Rods
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Mm.474941
RefSeq NM_030017 XM_006516372
OMIM
CCDS CCDS26009
HPRD
IMGT
MGI ID
MGI Symbol
EMBL
GenPept
RNA Seq Atlas