GAR1

Gene

GAR1 ribonucleoprotein

HGNCHGNC:14264 EnsemblENSG00000109534 NCBI Gene54433

Locus: gene with protein productLocation: 4q25

Also known as

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

Also known asNOLA1

View full nomenclature history (3)

Previous symbolsNOLA1

Previous namesnucleolar protein family A, member 1 (H/ACA small nucleolar RNPs), GAR1 ribonucleoprotein homolog (yeast)

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.

Neurodegenerative Diseases

Prostate carcinoma

Autosomal dominant primary hypomagnesemia with hypocalciuria

Hyperkalemic periodic paralysis

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.

H/ACA ribonucleoprotein complexTelomerase holoenzyme subunits

Provenance

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

Open TargetsGene–disease associations from the Open Targets Platform.