SNURF (NM_022804) Human Untagged Clone

CAT#: SC112432

SNURF (untagged)-Human SNRPN upstream reading frame (SNURF), transcript variant 2

Specifications

Product Data

• Type: Human Untagged Clone
• Tag: Tag Free
• Symbol: SNURF
• Synonyms: SNRPN upstream reading frame; SNRPN upstream reading frame protein
• Vector: pCMV6-XL5
• E. coli Selection: Ampicillin (100 ug/mL)
• Mammalian Cell Selection: None
• Sequence Data:
  Fully Sequenced ORF

  >OriGene ORF within SC112432 sequence for NM_022804 edited (data generated by NextGen Sequencing)
  ATGGAGCGGGCAAGGGATCGCTTACACCTGAGACGAACTACAGAACAGCACGTACCAGAG
  GTGGAAGTCCAAGTCAAACGCAGAAGGACTGCCTCACTGAGCAACCAAGAGTGTCAGTTG
  TACCCGAGGCGTTCTCAGCAGCAGCAAGTACCTGTGGTGGATTTCCAGGCTGAACTGAGG
  CAGGCATTCTTAGCTGAGACACCAAGAGGTGGTTAA
  
  Clone variation with respect to NM_022804.2
  
  5' Read Nucleotide Sequence

  >OriGene 5' read for NM_022804 unedited
  TAATACGACTCACTATAGGGCGGCCGCGAATTCGGCACGAGGGATGCCTGACGCATCTGT
  CTGAGGAGCGGTCAGTGACGCGATGGAGCGGGCAAGGGATCGCTTACACCTGAGACGAAC
  TACAGAACAGCACGTACCAGAGGTGGAAGTCCAAGTCAAACGCAGAAGGACTGCCTCACT
  GAGCAACCAAGAGTGTCAGTTGTACCCGAGGCGTTCTCAGCAGCAGCAAGTACCTGTGGT
  GGATTTCCAGGCTGAACTGAGGCAGGCATTCTTAGCTGAGACACCAAGAGGTGGTTAAAG
  CCATATTGGAGTAGCGAGGAATCTGATTCCAAGCAAAAACCAGGCTCCATCTACTCTTTG
  AAGCTTCTGCCCAGCTTGCATTGTTTCTAGGAGAACCTGCGTCATACCTTTATCTATAGC
  CTTCCCCTAGGTCTTCAGAAGCATCAAGTTTTAACTGTGGACATTGGATTTGGTGGAACA
  GCAATCATGACTGTTGGCAAGAGTAGCAAGATGCTGCAGCACATTGACTATAGAATGAGA
  TGTATCCTGCAAGATGGCCGAATCTTCATTGGCACCTTTAAGGCTTTTGACAAGCATATG
  AATTTGATCCTCTGTGATTGTGATGAGTTCAGAAAGATCAAGCCAAAGAATGCGAAGCAA
  CCAGAGCGTGAAAAAAGCGGGTTTTGGGGTCTGGGTGGTGCTGCGTGGGGAGAACTTGGT
  ATCCATGACTGTGNGAGGNGCCCACCCCCCANAGATACTGGCATTGCTCGGNNTACCCAC
  TTGCTGAGCTGCTGGNAGCCCCTGNNNGGTTGTAGGGCANCTGTAAAAGGATACCANCTG
  GTGTGCCATTCCCCAGCCCCCTGCTGATNGNCAGCCCTGTCCAAGGGATTGGGGGACATN
  CCANCAGTATGACTCCAGGNA
  
• Restriction Sites: NotI-NotI
• ACCN: NM_022804
• ORF Size: 216 bp
• OTI Disclaimer: Our molecular clone sequence data has been matched to the reference identifier above as a point of reference. Note that the complete sequence of our molecular clones may differ from the sequence published for this corresponding reference, e.g., by representing an alternative RNA splicing form or single nucleotide polymorphism (SNP).

Reference Data

• RefSeq: NM_022804.1, NP_073715.1
• RefSeq Size: 347
• RefSeq ORF: 216
• Locus ID: 8926
• Protein Families: Stem cell - Pluripotency
• Gene Summary: This gene is located within the Prader-Willi Syndrome critical region on chromosome 15. Transcripts produced from this gene initiate at an imprinting center and are paternally-imprinted. These transcripts may be bicistronic and also encode SNRPN (small nuclear ribonucleoprotein polypeptide N) from a downstream open reading frame. The small protein represented by this gene is encoded by an evolutionarily-conserved upstream open reading frame and is localized to the nucleus. Extensive alternative splicing and promoter usage occurs in this region and the full-length nature of some of these transcripts has not been determined. Alterations in the imprinting center are associated with parental imprint switch failure, which may cause Angelman syndrome or Prader-Willi syndrome. [provided by RefSeq, Mar 2017]
  Transcript Variant: This variant (2) lacks multiple 3' exons and contains an alternate 3' UTR compared to variant 1. This variant is monocistronic and cannot encode the SNRPN protein.