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GARIN1A

Gene

golgi associated RAB2 interactor 1A

HGNCHGNC:27998EnsemblENSG00000205085NCBI Gene346653
Locus: gene with protein productLocation: 7q32.1

Also known as

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

Also known asFAM137B · FAM71F2 · GARI
View full nomenclature history (6)
Previous symbolsFAM137B, FAM71F2
Alias symbolsGARI
Previous namesfamily with sequence similarity 137, member B, family with sequence similarity 71 member F2
Alias namesGolgi-associated RAB2B interactor

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.

Diabetes Mellitus, Type 2
Shock, Septic
Atrial Fibrillation
Connective Tissue Diseases
Corneal Ulcer
Migraine with Aura

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.

Golgi associated RAB2 interactor family

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2024-01-31.
Open TargetsGene–disease associations from the Open Targets Platform.