GRK1

Gene

G protein-coupled receptor kinase 1

HGNCHGNC:10013 EnsemblENSG00000185974 NCBI Gene6011

Locus: gene with protein productLocation: 13q34

Also known as

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

Also known asRHOK · GPRK1 · RK

View full nomenclature history (4)

Previous symbolsRHOK

Alias symbolsGPRK1, RK

Previous namesrhodopsin kinase

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.

Congenital stationary night blindness

Autoimmune disorder of central nervous system

Genetic Diseases, Inborn

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.

G protein-coupled receptor kinase family

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.

Open TargetsGene–disease associations from the Open Targets Platform.