MYRIP

Gene

myosin VIIA and Rab interacting protein

HGNCHGNC:19156 EnsemblENSG00000170011 NCBI Gene25924

Locus: gene with protein productLocation: 3p22.1

Also known as

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

Also known asDKFZp586F1018 · exophilin-8 · SLAC2-C · SLAC2C

View full nomenclature history (7)

Alias symbolsDKFZp586F1018, exophilin-8, SLAC2-C, SLAC2C

Alias namessynaptotagmin-like protein homologue lacking C2 domains-c, rab effector MYRIP, Slp homologue lacking C2 domains

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.

Sleep Apnea Syndromes

Nervous System Diseases

Intracranial Aneurysm

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.

A-kinase anchoring proteins

Provenance

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

Open TargetsGene–disease associations from the Open Targets Platform.