NAPA

Gene

NSF attachment protein alpha

HGNCHGNC:7641 EnsemblENSG00000105402 NCBI Gene8775

Locus: gene with protein productLocation: 19q13.33

Also known as

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

View full nomenclature history (3)

Previous namesN-ethylmaleimide-sensitive factor attachment protein, alpha

Alias namesalpha SNAP, alpha soluble NSF attachment protein

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.

Pre-Eclampsia

Vitiligo

Autosomal recessive primary microcephaly

Genetic developmental and epileptic encephalopathy

Genetic central nervous system malformation

Megalencephaly - polymicrogyria - postaxial polydactyly - hydrocephalus

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.