Back to discover

RIMS4

Gene

regulating synaptic membrane exocytosis 4

HGNCHGNC:16183EnsemblENSG00000101098NCBI Gene140730
Locus: gene with protein productLocation: 20q13.12

Also known as

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

Also known asC20orf190 · dJ781B1.3
View full nomenclature history (3)
Previous symbolsC20orf190
Alias symbolsdJ781B1.3
Previous nameschromosome 20 open reading frame 190

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.

Ovarian dysfunction
Metabolic Syndrome
Amelogenesis imperfecta
Stiff-Person Syndrome

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 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.