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SNRPN

—Small Nuclear Ribonucleoprotein Polypeptide N

Chromosome: 15

Location: 15:24823637-24978723

OMIM: 182279

Ensembl: ENSG00000128739

Official·OMIM:182279 Official·ENSG00000128739

Encodes small nuclear ribonucleoprotein polypeptide. Loss of paternal allele causes Prader-Willi syndrome.

Treatment Roadmap — SNRPN

Preclinical

Phase 1

Phase 2

Phase 3

Approved

Clinical trials have approximately 10% success rate. This roadmap shows the current status, not guaranteed outcomes.

Associated Diseases

Prader-Willi Syndrome

paternal_imprintingPrevalence: 1/15000neurological

Official·OMIM:176270 Official·ORPHA739

Summary

Clinical Trial

Approved Therapy

Registered Variant