DNM1

Gene

dynamin 1

HGNCHGNC:2972 EnsemblENSG00000106976 NCBI Gene1759

Locus: gene with protein productLocation: 9q34.11

Also known as

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

Also known asDNM

View full nomenclature history (1)

Previous symbolsDNM

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.

Lennox-Gastaut syndrome

Genetic Diseases, Inborn

Genetic developmental and epileptic encephalopathy

Undetermined early-onset epileptic encephalopathy

Sleep Initiation and Maintenance Disorders

Infantile spasms

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.

Pleckstrin homology domain containingDynamins

Provenance

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

Open TargetsGene–disease associations from the Open Targets Platform.