TBLR1 (TBL1XR1) (AF267864) Human Untagged Clone

CAT#: SC105965

(untagged)-Human DC42 mRNA, complete cds

Specifications

Product Data

• Type: Human Untagged Clone
• Tag: Tag Free
• Symbol: TBL1XR1
• Synonyms: C21|DC42|IRA1|MRD41|TBLR1
• Vector: pCMV6-XL4
• E. coli Selection: Ampicillin (100 ug/mL)
• Mammalian Cell Selection: None
• Sequence Data:
  Fully Sequenced ORF

  >NCBI ORF sequence for AF267864, the custom clone sequence may differ by one or more nucleotides
  
  
  ATGCAGCGCTACAATTTTCATTATCTTAAGTACATTGTACATTTCTACAGAACCTGTGATTATTCTCGCA
  TGATAAGGATGGTACTTGCATATGGTGAATTACTACTGTTGACAGTTTCCGCAGAAATCCTATTTCAGTG
  GACCAACATTGTGGCATGGCAGCAAATGCCAACATTTTGTGGAATAGCAGCAAATCTACAAGAGACCCTG
  GTTGGTTTTTCGTTTTGTTTTCTTTGTTTTTTCCCCCTTCTCCTGAATCAGCAGGGATGGAAGGAGGGTA
  GGGAAGTTATGAATTACTCCTTCCAGTAG
  
  
  5' Read Nucleotide Sequence

  >OriGene 5' read for AF267864 unedited
  TCAAATTTTGTATACGACTCACTATAGGCGGCCGCGAAATTCGCACGAGAATACATGAAG
  GTTTTTTGCTTTTTGACATACGAAAATGTCAAGAGAAAGGCCAAAGATTTGTACTTTTTC
  ACTTACAAAGCACTCCTTTTTCCCTTAAACTTCTTTCTGTCAAATTAGATTTAATGAGAG
  AGTACTATTTTTAAGGAGCTATCTGTTTATGTAGAATGATTTTGTTAAGAGTAATGTAAA
  CTATTATTGAGTAGAGGCCTAAAGAGGACTGTGCATTTTTGCTATTTAAAGGAATCACAA
  ATGATCATACTTAAGTGAGCAAAAATGACAAGTTTTACTAGCTAAGTAGAGAAATAAATC
  TCAAATGCAGCGCTACAATTTTCATTATCTTAAGCACATTGTACATTTCTACAGAACCTG
  TGATTATTCTCGCATGATAAGGATGGTACTTGCATATGGTGAATTACTACTGTTGACAGT
  TTCCGCAGAAATCCTATTTCAGTGGACCAACATTGTGGCATGGCAGCAAATGCCAACATT
  TTGTGGAATAGCAGCAAATCTACAAGAGACCCTGGTTGGTTTTTCGTTTTGTTTTCTTTG
  TTTTTTCCCCCTTCTCCTGAATCAGCAGGGATGGAAGGAGGGTANGGAAGTTACGAATTA
  CTCCTTCCAATAGTAGCTCTGAAGTGTCACATTTAATATCAGTTTTTTTTTAACATGATT
  CTAGTTAAATGTAGAAGAGAGAAGAAGAGGAAAGTGTCACTTTTTTTATACACTGATTTA
  GAAATTTGATGTCTTATATCAGTAGTTCTGAGGTATTGATAGCTTGCCTTATTTCTGCCT
  TTTACGTGACAGTGTTGAAGCAGGGTGAATAACTANGGCATATATTTTTTTTTTTTGTAA
  GCTGTTCAATGAGTTTTCTTTGGGATTTCCGGTAAGTTCAGGAAACATCTGCCATGTGNT
  CTAGNCGGAGTACCTAAC
  
  3' Read Nucleotide Sequence

  >OriGene 3' read for AF267864 unedited
  NNNNGGGTAAGACTAAGNACCGCGNCCGCATNCTANGATCGAATTTTTTTTTTTTTTTTT
  AATATCAAAAATATTTTATTCTGGGACTCTTTCAGACTGATTCAAATACAGTTGTCAAAG
  CAATACAATGCAAAGGGGAACTGCAACAACAACAACAACAAGAAATGTGCCTAGAAAGGA
  TAAAAGGGTCACTGGGGACAAATCATTGTGATGTGGAACTAAAATACGTCGTAAGTGTAA
  TTAACATGGTCCAGGACAGCACAGAACATCTACATCAGTCTTCCTTACACAATAATCATG
  AAAACTGAACAATGAAGTTCTTTAACATGTACAAAAACCTGTCATGGGCTGGTTTACACT
  TTTACAACAGTTTTAAAGTTAACTGGATAACTAAAGAAATGATGCAGACATTTTAATCCA
  GTGCTATAGGTAGGCTCACAGAATTAGACCCAAAGGATTTGTAAAAACAAAAATGGAAAC
  AGTATAGCTACAATGTCAAAGTCAGGAAAGAAGAAAATTTACTTCCGTATTCAAGGATTA
  CAGAGCTACAAATGCAGTCTGTGTGTTTTTGTTTGTAATGAGATGGATAAGTACATCAGA
  CTAGATACAACATGCAGAATGTTTTCCTGAACTTATCCGGAAATTCCAAAGAAAACATCA
  TGAAACAGCTTACAAAAAAAAAAAAATATATGCCCTAGTTATTCACCCTGCTTCAACACT
  GTCAACGTAAAGGCAGAAATAAAGCAAGCTATCAATACCTCAGAACTACTGATATAAGAC
  ATCAAATTTCTAAATCAGTGTATTAAAAAAGTGAACACTTCCTCTTTTCTTCTCTCTTCT
  ACATTTAACTAGAATCATGTTTAAAAAAACTGATAATTAATGTGACACTTTCAA
  
• Restriction Sites: NotI-NotI
• ACCN: AF267864
• ORF Size: 1632 bp
• Insert Size: 1410
• 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: AF267864.1, AAG44733.1
• RefSeq Size: 1632
• RefSeq ORF: 1632
• Locus ID: 79718
• Protein Families: Druggable Genome, Transcription Factors
• Protein Pathways: Wnt signaling pathway
• Gene Summary: This gene is a member of the WD40 repeat-containing gene family and shares sequence similarity with transducin (beta)-like 1X-linked (TBL1X). The protein encoded by this gene is thought to be a component of both nuclear receptor corepressor (N-CoR) and histone deacetylase 3 (HDAC 3) complexes, and is required for transcriptional activation by a variety of transcription factors. Mutations in these gene have been associated with some autism spectrum disorders, and one finding suggests that haploinsufficiency of this gene may be a cause of intellectual disability with dysmorphism. Mutations in this gene as well as recurrent translocations involving this gene have also been observed in some tumors. [provided by RefSeq, Mar 2016]