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RDH12

Gene

retinol dehydrogenase 12

HGNCHGNC:19977EnsemblENSG00000139988NCBI Gene145226
Locus: gene with protein productLocation: 14q24.1

Also known as

Symbols and names change; identity (the HGNC ID) does not. Previous and alternative forms are kept distinct.

Also known asFLJ30273 · SDR7C2 · LCA13 · RP53
View full nomenclature history (7)
Alias symbolsFLJ30273, SDR7C2, LCA13, RP53
Previous namesretinol dehydrogenase 12 (all-trans and 9-cis), retinol dehydrogenase 12 (all-trans/9-cis/11-cis)
Alias namesshort chain dehydrogenase/reductase family 7C, member 2

Associated diseases

via associated_with

Diseases linked to this gene through the canonical GENE→DISEASE (associated_with) relation, drawn from Open Targets' top-ranked associations by overall score — not the full association set. Disease-level detail lives on each disease's own page.

Leber Congenital Amaurosis
Retinitis Pigmentosa
Cone rod dystrophy
Cone-rod dystrophy

Drawn from Open Targets’ top 10 associations by overall score for this gene — the subset resolved to a canonical disease. Lower-ranked associations, and diseases not yet canonicalised, are not shown.

Gene family

HGNC gene-group membership.

Short chain dehydrogenase/reductase superfamily

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.
Open TargetsGene–disease associations from the Open Targets Platform.