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DTNA

Gene

dystrobrevin alpha

HGNCHGNC:3057EnsemblENSG00000134769NCBI Gene1837
Locus: gene with protein productLocation: 18q12.1

Also known as

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

Also known asD18S892E · DTN · DTN-1 · DTN-2 · DTN-3 · DRP3
View full nomenclature history (8)
Alias symbolsD18S892E, DTN, DTN-1, DTN-2, DTN-3, DRP3
Previous namesdystrobrevin, alpha
Alias namesdystrophin-related protein 3

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.

Atrial Fibrillation
Muscular dystrophy
Alcohol drinking
Cardiomyopathy, Dilated
Meniere's Disease

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.

Zinc fingers ZZ-type

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-03-15.
Open TargetsGene–disease associations from the Open Targets Platform.