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STXBP2

Gene

syntaxin binding protein 2

HGNCHGNC:11445EnsemblENSG00000076944NCBI Gene6813
Locus: gene with protein productLocation: 19p13.2

Also known as

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

Also known asUNC18B · Hunc18b · Unc18-2 · MUNC18-2
View full nomenclature history (4)
Alias symbolsUNC18B, Hunc18b, Unc18-2, MUNC18-2

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
Genetic Diseases, Inborn
Neuralgia
Kartagener Syndrome

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.

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.
Open TargetsGene–disease associations from the Open Targets Platform.