RBM10 (NM_152856) Human Untagged Clone

CAT#: SC109927

RBM10 (untagged)-Human RNA binding motif protein 10 (RBM10), transcript variant 2

Specifications

Product Data

• Type: Human Untagged Clone
• Tag: Tag Free
• Symbol: RBM10
• Synonyms: DXS8237E; GPATC9; GPATCH9; S1-1; TARPS; ZRANB5
• Vector: pCMV6-XL6
• E. coli Selection: Ampicillin (100 ug/mL)
• Mammalian Cell Selection: None
• Sequence Data:
  Fully Sequenced ORF

  >NCBI ORF sequence for NM_152856, the custom clone sequence may differ by one or more nucleotides
  
  
  ATGGAGTATGAAAGACGTGGTGGTCGTGGTGACAGGACTGGCCGCTATGGAGCCACTGACCGCTCGCAGG
  ATGATGGTGGGGAGAACCGCAGCCGAGACCACGACTACCGGGACATGGACTACCGTTCATATCCTCGCGA
  GTATGGCAGCCAGGAGGGCAAGCATGACTATGACGACTCATCTGAGGAGCAGAGTGCGGAGATCCGTGGC
  CAGCTGCAGTCGCACGGCGTGCAAGCACGGGAGGTTCGGCTGATGCGGAACAAATCTTCAGGTCAGAGCC
  GGGGCTTCGCCTTCGTCGAGTTTAGTCACTTGCAGGACGCTACACGATGGATGGAAGCCAATCAGCACTC
  CCTCAACATCCTGGGCCAGAAGGTGTCGATGCACTACAGTGACCCCAAGCCCAAGATCAATGAGGACTGG
  CTGTGCAATAAGTGTGGCGTCCAGAACTTCAAACGCCGAGAGAAGTGCTTCAAATGTGGCGTGCCCAAGT
  CAGAGGCAGAGCAGAAGCTGCCCCTCGGCACGAGGCTGGATCAGCAGACACTGCCACTGGGTGGCCGGGA
  GCTGAGCCAGGGCCTGCTTCCCCTGCCGCAGCCCTACCAGGCCCAGGGAGTCCTGGCCTCCCAAGCCCTG
  TCACAGGGCTCGGAGCCAAGCTCAGAGAACGCCAATGACACCATCATTTTGCGCAACCTGAACCCACACA
  GCACCATGGATTCCATCCTGGGGGCCCTGGCACCCTACGCGGTGCTGTCCTCCTCCAACGTGCGCGTCAT
  AAAGGACAAGCAGACCCAACTGAACCGCGGCTTTGCCTTCATCCAGCTCTCCACCATCGAGGCAGCCCAG
  CTGCTGCAGATCCTGCAGGCCCTGCACCCACCACTCACTATCGACGGCAAGACCATCAATGTTGAGTTTG
  CCAAGGGTTCTAAGAGGGACATGGCCTCCAATGAAGGCAGTCGCATCAGTGCTGCCTCTGTGGCCAGCAC
  TGCCATTGCTGCGGCCCAGTGGGCCATCTCACAGGCCTCCCAAGGTGGGGAGGGTACCTGGGCCACCTCC
  GAGGAGCCGCCGGTCGACTACAGCTACTACCAACAGGATGAGGGCTATGGCAACAGCCAGGGCACAGAGT
  CTTCCCTCTATGCCCATGGCTACCTCAAGGGCACCAAGGGCCCTGGCATCACTGGAACCAAAGGGGATCC
  CACTGGAGCAGGTCCCGAGGCCTCCCTAGAGCCTGGGGCCGACTCTGTGTCGATGCAGGCTTTCTCTCGC
  GCCCAGCCTGGTGCTGCTCCTGGCATCTACCAACAATCAGCCGAGGCGAGCAGTAGCCAGGGCACTGCTG
  CCAACAGCCAGTCGTATACCATCATGTCACCCGCTGTGCTCAAATCTGAGCTCCAGAGCCCTACCCATCC
  TAGTTCTGCTCTCCCACCGGCTACCAGCCCCACTGCCCAGGAATCCTACAGCCAGTACCCTGTTCCCGAC
  GTCTCTACCTACCAGTACGATGAGACCTCCGGCTACTACTATGACCCCCAGACCGGCCTCTACTATGACC
  CCAACTCCCAGTATTACTACAATGCTCAGAGCCAGCAGTACCTGTACTGGGATGGGGAGAGGCGGACCTA
  TGTTCCCGCCCTGGAGCAGTCGGCCGACGGACATAAGGAGACAGGGGCACCCTCGAAGGAGGGCAAAGAG
  AAGAAGGAGAAGCACAAGACCAAGACAGCTCAACAGATTGCCAAGGACATGGAACGCTGGGCCCGCAGTC
  TCAACAAACAAAAAGAAAACTTCAAAAATAGCTTCCAGCCTATCAGCTCCCTGCGAGATGACGAGAGGCG
  GGAGTCAGCCACTGCAGATGCTGGCTATGCCATCCTCGAGAAGAAGGGAGCACTAGCCGAGAGACAGCAC
  ACCAGCATGGATCTCCCGAAATTGGCCAGTGACGACCGCCCAAGCCCTCCGCGAGGACTGGTGGCAGCCT
  ACAGCGGGGAGAGTGACAGTGAGGAGGAGCAGGAGCGTGGGGGCCCTGAGCGGGAGGAGAAGCTCACCGA
  CTGGCAGAAGCTGGCCTGTCTGCTCTGCCGACGCCAGTTCCCCAGCAAAGAGGCGCTCATCCGGCACCAG
  CAGCTCTCAGGGCTCCACAAGCAAAACCTTGAGATTCACCGGCGAGCCCACTTGTCAGAAAACGAGCTAG
  AAGCACTAGAGAAGAATGACATGGAGCAAATGAAGTACCGGGACCGTGCAGCTGAACGCAGAGAAAAGTA
  TGGCATCCCCGAGCCGCCAGAGCCCAAGAGGAGGAAGTACGGCGGCATATCCACAGCCTCTGTAGACTTC
  GAGCAGCCTACTCGGGACGGGCTGGGCAGTGACAACATTGGCAGTCGGATGCTGCAGGCCATGGGCTGGA
  AAGAGGGCAGCGGCCTGGGCCGCAAGAAGCAGGGCATTGTAACGCCTATCGAGGCCCAAACACGGGTGCG
  GGGCTCCGGCCTGGGTGCACGGGGCAGCTCCTACGGGGTCACCTCAACCGAGTCCTACAAGGAGACACTG
  CACAAGACAATGGTGACCCGCTTCAACGAGGCCCAGTGA
  
  
  5' Read Nucleotide Sequence

  >OriGene 5' read for NM_152856 unedited
  ACTTCCGCTCCCGTTGCCGCATTGGGCGGTAGGCGTGTACGGTGGGAGGTCTATATAAGC
  AGAGCTCATTTAGGTGACACTATAGAATACAAGCTACTTGTTCTTTTTGCAGCGGCCGCG
  TGAGCTGGTGACTGTGGCCGGCTGGGAGTAGGCGGCAGTGAGTTTCCCTGGGAGGGCAGC
  GCGCTTGGCGCTTCTCCCCTCCCCCCGATCTGCCTCCAGTCTCGGACTTGGTTGTTGCGC
  GCTCCGGCTCCGGCTGAGCTGGGAGAGTTGGAGGAGGTGGCGGCGGGCAGAGGTGATGTC
  TGGGAGCCCTTCCTTGACAGCCCGGGCCGAGAAGAGTCCCTGCAGGAAGCATCACCCAGT
  CTGGCAGATCATGGTAGCAGCAGCGGGGGTGGCTGGGAAGTGAAACGGAGCCAGCGGCTG
  AGGAGGGGCCCCAGCAGCCCCCGAAGGCCCTATCAGGACATGGAGTATGAAAGACGTGGT
  GGTCGTGGTGACAGGACTGGCCGCTATGGAGCCACTGACCGCTCGCAGGATGATGGTGGG
  GAGAACCGCAGCCGAGACCACGACTACCGGGACATGGACTACCGTTCATATCCTCGCGAG
  TATGGCAGCCAGGAGGGCAAGCATGACTATGACGACTCATCTGAGGAGCAGAGTGCGGAG
  ATCCGTGGCCAGCTGCAGTCGCACGACGTGCAAGCACGGGAGGTTCGGCTGATGCGGAAC
  ANATCTTCAGGTCAGAGCCGGNGCTTCGCCTTCGTCGAGTTTAGTCACTTGCANGACGCT
  ACACGATGGATGGAAGCCAATCAGCACTCCCNTCACATCCTGNGCCAGAAGGTGTCGATG
  CACTACAGTGACCCCCAGCCCCNAGATCATGANGACTGGNCTGTGCATAAGTGTGGCGTC
  CAGAACTTNCAACGCCGANAGAAGTGCTTCAATGTGGCGTGCC
  
  3' Read Nucleotide Sequence

  >OriGene 3' read for NM_152856 unedited
  AAAAACCCTAGCATGNACCTGCGGCCGCTTTCTANGATCGGTTTTTTTTTTTTTTTTTTG
  CAGACTTTTCATCTTTTTTACAAAACAGACGTGATCCCAGCCCAATTTTCCAACAAAAGT
  CACCACCTCAATTTGATTTGGTCAAGCCCTCTCTGGCTGGGGAGTGGGCTGGCCGACAAG
  AGCAAGGCCCCGTCCCAGCCATCCAACACTCTGTCCTTCCCTGCCCCAGGATGGACACCC
  AACATGTGGAGAAGTTGCTCTTGAAGCTGCTCACTGGGCCTCGTTGAAGCGGGTCACCAT
  TGTCTTGTGCAGTGTCTCCTTGTAGGACTCGGTTGAGGTGACCCCGTAGGAGCTGCCCCG
  TGCACCCAGGCCGGAGCCCCGCACCCGTGTTTGGGCCTCGATAGGCGTTACAATGCCCTG
  CTTCTTGCGGCCCATGCCGCTGCCCTCTTTCCAGCCCATGGCCTGCAGCATCCGACTGCC
  AATGTTGTCACTGCCCAGCCCGTCCCGAGTAGGCTGCTCGAAGTCTACAGAGGCTGTGGA
  TATGCCGCCGTACTTCCTCCTCTTGGGCTCTGGCGGCTCGGGGATGCCATACTTTTCTCT
  GCGTTCAGCTGCACGGTCCCGGTACTTCATTTGCTCCATGTCATTCTTCTCTAGTGCTTC
  TAGCTCGTTTTCTGACAAGTGGGCTCGCCGGTGAATCTCAAGGTTTTGCTTGTGGAGCCC
  TGAGAGCTGCTGGTGCCCGATGAGCGCCTCTTTGCTGGGGAACTGGCGTCGGCAGAGCAG
  ACAAGCCAGCTTCTGCCAGTCGGTGAGCTTCTCCCTCCCGTCAGGGGCCCCAAGCTTCTG
  GTTCTNCTA
  
• Restriction Sites: NotI-NotI
• ACCN: NM_152856
• ORF Size: 2559 bp
• Insert Size: 3300
• 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_152856.1, NP_690595.1
• RefSeq Size: 3190
• RefSeq ORF: 2559
• Locus ID: 8241
• Domains: G-patch, RRM, zf-RanBP, zf-C2H2
• Protein Families: Druggable Genome
• Gene Summary: This gene encodes a nuclear protein that belongs to a family proteins that contain an RNA-binding motif. The encoded protein associates with hnRNP proteins and may be involved in regulating alternative splicing. Defects in this gene are the cause of the X-linked recessive disorder, TARP syndrome. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Mar 2011]
  Transcript Variant: This variant (2) lacks an in-frame exon and uses and alternate splice site in the coding region, compared to variant 1. The encoded isoform (2) is shorter than isoform 1.