Back to discover

RIMS1

Gene

regulating synaptic membrane exocytosis 1

HGNCHGNC:17282EnsemblENSG00000079841NCBI Gene22999
Locus: gene with protein productLocation: 6q13

Also known as

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

Also known asRAB3IP2 · CORD7 · RIM · KIAA0340 · RIM1
View full nomenclature history (7)
Previous symbolsRAB3IP2, CORD7
Alias symbolsRIM, KIAA0340, RIM1
Previous namesRAB3 interacting protein 2
Alias namesRab3-interacting molecule

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.

Cone rod dystrophy
Alcohol drinking
Cone-rod dystrophy
Diabetic Ketoacidosis
Hypertension, Portal
Autism Spectrum Disorder

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.

Regulating synaptic membrane exocytosis familyPDZ domain containing

Provenance

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