Back to discover

REEP6

Gene

receptor accessory protein 6

HGNCHGNC:30078EnsemblENSG00000115255NCBI Gene92840
Locus: gene with protein productLocation: 19p13.3

Also known as

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

Also known asC19orf32 · DP1L1 · FLJ25383 · Yip2f · TB1
View full nomenclature history (8)
Previous symbolsC19orf32
Alias symbolsDP1L1, FLJ25383, Yip2f, TB1
Previous nameschromosome 19 open reading frame 32
Alias namespolyposis locus protein 1-like 1, deleted in polyposis 1-like 1

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.

Retinitis Pigmentosa
Retinal Dystrophies
Genetic Diseases, Inborn
Optic Atrophy
Cone rod dystrophy
Color Vision Defects
Leber Congenital Amaurosis

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.

Receptor accessory proteins

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-09-18.
Open TargetsGene–disease associations from the Open Targets Platform.