small nuclear ribonucleoprotein polypeptide SmN gene

15q11.2 Pathology: - maternal imprinting of the SmN gene suggests that paternal absence of SmN is responsible for the Prader-Willi syndrome phenotype

Related

Prader-Willi syndrome small nuclear ribonucleoprotein associated protein N (SmN) [tissue-specific slicing factor] (SnRPN)

Properties

TEMPLATE-FOR: messenger RNA TEMPLATE-FOR: snRNP polypeptide SmN MOTIF: transcription factor binding site transcriptional start site exon (8) intron (7) transcriptional termination site