SNRPN

Gene

small nuclear ribonucleoprotein polypeptide N

HGNCHGNC:11164 EnsemblENSG00000128739 NCBI Gene6638

Locus: gene with protein productLocation: 15q11.2

Also known as

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

Also known asPWCR · SMN · SM-D · HCERN3 · SNRNP-N · SNURF-SNRPN · RT-LI

View full nomenclature history (11)

Previous symbolsPWCR

Alias symbolsSMN, SM-D, HCERN3, SNRNP-N, SNURF-SNRPN, RT-LI

Previous namesPrader-Willi syndrome chromosome region

Alias namestissue-specific splicing protein, SM protein N, small nuclear ribonucleoprotein N

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.

Prader-Willi syndrome

Neurodegenerative Diseases

Dengue

Intracranial Aneurysm

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.

Sm spliceosomal proteins

Provenance

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

Open TargetsGene–disease associations from the Open Targets Platform.