small nuclear ribonucleoprotein polypeptide SmN gene

Introduction

15q11.2

Pathology

• maternal imprinting of the SmN gene suggests that paternal absence of SmN is responsible for the Prader-Willi syndrome phenotype

More general terms

• unclassified gene

Additional terms

• Prader-Willi syndrome

Database

• Entrez gene: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&cmd=Retrieve&dopt=Graphics&list_uids=6638