STX19

Gene

syntaxin 19

HGNCHGNC:19300 EnsemblENSG00000178750 NCBI Gene415117

Locus: gene with protein productLocation: 3q11.2

Also known as

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

Also known asMGC21382

View full nomenclature history (1)

Alias symbolsMGC21382

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.

Fractures, Bone

Osteoporosis, Postmenopausal

Venous Thromboembolism

Heart Diseases

Diabetes Mellitus, Type 2

Diabetes Mellitus

Carcinoma, Renal Cell

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.

Syntaxins

Provenance

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

Open TargetsGene–disease associations from the Open Targets Platform.