SEPTIN10

Gene

septin 10

HGNCHGNC:14349 EnsemblENSG00000186522 NCBI Gene151011

Locus: gene with protein productLocation: 2q13

Also known as

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

Also known asSEPT10 · FLJ11619 · Septin-10

View full nomenclature history (4)

Previous symbolsSEPT10

Alias symbolsFLJ11619, Septin-10

Alias namessept1-like

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.

Nutritional deficiency disease

Alcohol drinking

Stroke

Placental abruption

Adenocarcinoma of Lung

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.

Septins

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-10-19.

Open TargetsGene–disease associations from the Open Targets Platform.