SNURF a highly basic 71-aa nuclear protein. Encoded with SNRPN on a polycistronic transcript. Play an important role in maintaining differentialy methylated DNA. The gene is imprinted, and disruption of imprinting plays a role in Prader-Willi syndrome (PWS). Translated in normal, but not PWS, human, and mouse tissues. Note: This description may include information from UniProtKB.
Protein type: Gene silencing; Transcription regulation
Chromosomal Location of Human Ortholog: 15q11.2
Cellular Component:  nuclear speck; nucleus
Reference #:  Q9Y675 (UniProtKB)
Alt. Names/Synonyms: SNRPN upstream reading frame; SNRPN upstream reading frame protein; SNURF
Gene Symbols: SNURF
Molecular weight: 8,412 Da
Basal Isoelectric point: 10.58  Predict pI for various phosphorylation states
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SNURF

Protein Structure Not Found.

Cross-references to other databases:  STRING  |  cBioPortal  |  Wikipedia  |  neXtProt  |  Protein Atlas  |  BioGPS  |  Pfam  |  Phospho.ELM  |  NetworKIN  |  UniProtKB  |  Entrez-Gene  |  GenPept  |  Ensembl Gene  |  Ensembl Protein