UNC13D

Gene

unc-13 homolog D

HGNCHGNC:23147 EnsemblENSG00000092929 NCBI Gene201294

Locus: gene with protein productLocation: 17q25.3

Also known as

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

Also known asMunc13-4

View full nomenclature history (2)

Alias symbolsMunc13-4

Previous namesunc-13 homolog D (C. elegans)

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.

Lymphohistiocytosis, Hemophagocytic

Neurodegenerative Diseases

Cardiovascular Diseases

Coronary Artery Disease

Genetic Diseases, Inborn

Metabolic Diseases

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.

UNC13 homologs

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2024-01-16.

Open TargetsGene–disease associations from the Open Targets Platform.