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Invitrogen
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Immunogen sequence: LRRTTEQHVPE VEVQVKRRRT ASLSNQECQL YPRRS
Highest antigen sequence identity to the following orthologs - mouse 97%, rat 94%.
SNURF is a highly basic protein localized to the nucleus. The evolutionarily constrained open reading frame of its gene is found on a bicistronic transcript which has a downstream ORF encoding the small nuclear ribonucleoprotein polypeptide N. The upstream coding region utilizes the first three exons of the transcript, a region that has been identified as an imprinting center. Multiple transcription initiation sites have been identified and extensive alternative splicing occurs in the 5' untranslated region but the full-length nature of these transcripts has not been determined. An alternate exon has been identified that substitutes for exon 4 and leads to a truncated, monocistronic transcript. Alternative splicing or deletion caused by a translocation event in the 5' UTR or coding region of this gene leads to Angelman syndrome or Prader-Willi syndrome due to parental imprint switch failure. The function of this protein is not yet known.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: Sm protein D; Sm protein N; Sm-D; Sm-N; Small nuclear ribonucleoprotein-associated protein N; snRNP-N; SNRPN upstream reading frame protein; Tissue-specific-splicing protein
基因别名: HCERN3; SMN; SNRPN; SNURF
UniProt ID: (Human) Q9Y675
Entrez Gene ID: (Human) 8926