SMNDC1 (NM_005871) Human Untagged Clone

CAT#: SC116456

SMNDC1 (untagged)-Human survival motor neuron domain containing 1 (SMNDC1)

Specifications

Product Data

• Type: Human Untagged Clone
• Tag: Tag Free
• Symbol: SMNDC1
• Synonyms: SMNR; SPF30; TDRD16C
• Vector: pCMV6-XL5
• E. coli Selection: Ampicillin (100 ug/mL)
• Mammalian Cell Selection: None
• Sequence Data:
  Fully Sequenced ORF

  >OriGene ORF within SC116456 sequence for NM_005871 edited (data generated by NextGen Sequencing)
  ATGTCAGAGGATTTAGCAAAGCAGCTGGCAAGCTACAAAGCTCAGCTCCAGCAAGTTGAA
  GCTGCATTATCTGGAAATGGAGAAAATGAAGATTTGCTAAAATTGAAGAAAGATTTACAA
  GAAGTTATAGAACTAACCAAAGACCTTCTGTCAACTCAACCTTCTGAGACGCTTGCAAGT
  TCAGACAGTTTTGCTTCTACTCAACCTACTCATTCATGGAAAGTAGGAGACAAGTGTATG
  GCAGTCTGGAGTGAAGATGGACAGTGTTATGAAGCGGAGATTGAGGAGATAGATGAAGAA
  AATGGCACCGCTGCAATCACCTTTGCTGGTTATGGCAATGCTGAAGTGACTCCACTGTTG
  AACCTCAAGCCTGTAGAAGAAGGAAGGAAGGCAAAGGAGGACAGTGGCAACAAACCCATG
  TCAAAAAAAGAAATGATTGCCCAGCAGCGTGAATATAAAAAGAAGAAAGCTTTGAAAAAA
  GCTCAGAGAATAAAAGAACTTGAGCAGGAAAGAGAGGACCAGAAAGTGAAATGGCAACAA
  TTCAACAACAGAGCCTATTCTAAAAACAAAAAAGGCCAGGTAAAGAGGAGTATTTTTGCT
  TCACCTGAGAGTGTGACTGGTAAAGTTGGAGTAGGAACCTGTGGAATTGCTGATAAACCT
  ATGACACAATATCAAGATACCTCTAAATACAATGTCAGGCATTTGATGCCTCAATAA
  
  Clone variation with respect to NM_005871.3
  
  5' Read Nucleotide Sequence

  >OriGene 5' read for NM_005871 unedited
  TTTTGTATACGACTCCTATAGGCGGCCCGCGAATTCGCACGAGGCCCCTCCCCCTCGCCG
  CCGACCGAGTTCTTCCTTTTCAGACCGGGTCGCCTTGCTGTCGTCGCGGTGATTTTCCTG
  CTACTGCTACTGCTGCTGCTGCCACCGCCACTACCACTGGGCTCATTTGCCCCGACCCCT
  TCCCGCCGCCCCGCCCCCAGCCCCACACAAGATGTCAGAGGATTTAGCAAAGCAGCTGGC
  AAGCTACAAAGCTCAGCTCCAGCAAGTTGAAGCTGCATTATCTGGAAATGGAGAAAATGA
  AGATTTGCTAAAATTGAAGAAAGATTTACAAGAAGTTATAGAACTAACCAAAGACCTTCT
  GTCAACTCAACCTTCTGAGACGCTTGCAAGTTCAGACAGTTTTGCTTCTACTCAACCTAC
  TCATTCATGGAAAGTAGGAGACAAGTGTATGGCAGTCTGGAGTGAAGATGGACAGTGTTA
  TGAAGCGGAGATTGAGGAGATAGATGAAGAAAATGGCACCGCTGCAATCACCTTTGCTGG
  TTATGGCAATGCTGAAGTGACTCCACTGTTGAACCTCAAGCCTGTAAAAGAAGGAAGGAA
  GGCAAAGGAGGACAGTGGCAACAAACCCATGTCAAAAAAAGAAATGATTGCCCAGCAGCG
  TGAATATAAAAAGAAGAAAGCTTTGAAAAAAGCTCAGAGAATAAAAGAACTTGAGCAGGA
  NAGAGAAGACCCAGAAGTGAAATGGCAAACATTCAACAACAGAGCCTATTCTAAAACANA
  AAAGCCAGGTAANAGAGAGTATTTTGCTTCACTGAGATGTGACTGGTAAAGTGAGTAGAA
  ACTGTGGAATGCTGATAACCTATGACACATATCAGA
  
  3' Read Nucleotide Sequence

  >OriGene 3' read for NM_005871 unedited
  CGGCCGCAATCTANAGTCGAGTTTTTTTTTTTTTTTTTTGAGATTTTAAAAACACTTTAT
  TTAATAAAAGTTAAACATACAAAACTGAAATAATACACATCCTAAAAATTACCTTCTTCC
  ATTAATAGGAAGACCCTTTTCTATGCATGTATTTGGCTTAAACTCAACTCAGGATAACTG
  TGATGATGTTCACTTACACCAACAAATGCAGACAACCTGATCTAATTAACAAAAATTACA
  AACAGCTAAATGAACATAATATACAGGGAAATTATCGTCAGATTAATGCACAAGAAATAC
  AAGAAATTTTTAATGATGAAATATTCAGTATTCTTGTTCATTAATTTAGCCTTGTGTTTT
  TACAAAAATAGTATCTACACTGTATACAGGGCTATACATCAGCTTTTTGTTCTCCCATAT
  AAACATCACACATCCAAAACATGGTACCACTGCCGTAAATGGAAAAAACAAAAAACAGGA
  AAAAAGCAAACATACAAAAAACAAAAACACCTTAGAAAAGGGAGCTCATCCTAAGGTTTC
  TTACATAAAACTAAGAGTACATAAAAATAAAACAGCTAGATCAATTTTAGAGATGGCCTA
  ATAGGCCTGGGAAACAAGTTATTGAGGAANAACCTCAAAACAAACTTTGCCATTTACAAA
  TTAACCTATCTTTAAGCTTAACTGAACGACAGCTAAGTTTTAAAGCTGAAATAAGAAAAA
  TGAANAGATCTCTTTTAGCAGGTTGGTGTTTTTGCCTTTGGTGNTCCAATGAATTGCTAG
  AGTATGTGTCAAGTTCAAAGCATCTGAAAATTCAAGTTACAACTTACAAAAAGTACACAC
  CATAGGTTAGTAGGCGCCTGATATANGAAGATCAATATCCATCTAGTGCTGNATGAACAC
  ATCTACAAAAGTGCTTTATCACANACTTTGAGGGACCGGNGTACTGAATATGAGAAAGTA
  ATGAAT
  
• Restriction Sites: ECoRI-NOT
• ACCN: NM_005871
• ORF Size: 717 bp
• Insert Size: 2050
• 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_005871.2, NP_005862.1
• RefSeq Size: 2033
• RefSeq ORF: 717
• Locus ID: 10285
• Domains: TUDOR
• Protein Families: Stem cell - Pluripotency
• Protein Pathways: Spliceosome
• Gene Summary: This gene is a paralog of SMN1 gene, which encodes the survival motor neuron protein, mutations in which are cause of autosomal recessive proximal spinal muscular atrophy. The protein encoded by this gene is a nuclear protein that has been identified as a constituent of the spliceosome complex. This gene is differentially expressed, with abundant levels in skeletal muscle, and may share similar cellular function as the SMN1 gene. [provided by RefSeq, Jul 2008]