FAM120C (NM_001300788) Human Untagged Clone

CAT#: SC337645

FAM120C (untagged) - Human family with sequence similarity 120C (FAM120C), transcript variant 3

Specifications

Product Data

• Type: Human Untagged Clone
• Tag: Tag Free
• Symbol: FAM120C
• Synonyms: CXorf17; ORF34
• Vector: pCMV6-Entry
• E. coli Selection: Kanamycin (25 ug/mL)
• Mammalian Cell Selection: Neomycin
• Sequence Data:
  Fully Sequenced ORF

  >NCBI ORF sequence for NM_001300788, the custom clone sequence may differ by one or more nucleotides
  
  
  ATGGGTGTCCAGGGCTTCCAAGAGTTCCTGGAGAAGCGCTGTCCCGGGGCCGTGGTGCCCGTGGACCTCC
  TAAAACTCGCGCGCACGGTCTCGCGCCAGCAGCAGCAGCAGCACTTGCACCGCCAGCTGCCGCCGACTGC
  AGCCCTAGCGCCCGGGGCTCCACGCGCCGCCAGGGGCTCCGTGCCTCTGCAACCGCCGCTTCCGCCCGCT
  GCCTTGGGTGCCTACTCCGGGGGCGCGGGGCCGACTCGGCACCATCACCCCGCTCACCACTTCCACCATC
  ATGGCCAAGCGCAGCCCGGGCTGCACCCTCCGCTGCCGCCGCCGCCGCCCCCTCAGCTGCCCGGGGCCCG
  GGTGCTGGTGGACGCCGGCTCGGCGCTGCCGCGGCTCTATGGCGGCTACCAGACGGATTGGGTGTGTGGC
  GGCCAATGGAACGCCATGCTGGGCTACTTGTCAGCGCTGTGCCAGGCTTGTGCCTATCCTGGCGGCGACG
  GCCTGGAGCTCGTGGTCATGTTCCCGGGGGGCCTGGGCAAGGACCGGCTGGCCGAGTGGGGCCGTCGGTG
  CCAGGCCGAGCGGCAGACAGCGCAACTGATCGTGGGACACGTGGGCAACAAGGGCACCCCTCCACCGCGG
  GCCTGGTTCCTGCCACCGGCCTGCCTGAGCCACTGCGTGAGGCTAGCACTCATCCGCTTCCGGGTCAAGG
  TCTTTCAGAGCCTTGAAGACCACCATTTGGAAGTGGTGGCGTTTTTCAGGGAAAATGGCTTCCATGGCCT
  TCTTGCCCATGACTCCGAGTATGCTCTCTACAATATTCCCTCTTACTACAGTTCCCATGCTCTGAAACTG
  AGCTGGAATGGGAAGAACCTCACTACCAACCAGTTCCTGATGCAAGAAGTAGCCAAGCAGCTGGGCCTGA
  AGAGGATGAATTTCCCCATATTTGCTGCACTGCTAGGTAACCACATCCTCCCAGATGAGGACCTGGCTGC
  TTTTCACTGGAGCCTCTTGGGACCAGAACATCCTCTTGCATCACTTAAGGTTCGAGCTCATCAGCTGGTT
  CTTCCTCCCTGTGACGTGGTGATCAAGGCTGTTTCTGAGTATGTCAGTTCCATCAAAGATCCCTCAAACC
  TGGATGTAGTTGGGAAGGATGTTTTCAAACAGTCTCAGTCCAGGACAGAAGATAAAATAGAGCGATTCAA
  GAAAGCAGTTGAGTATTATTCAGTCACAACCAAACTCTCTTCGCTGCCAGTGGGTCCCTCCTTTCTAGGT
  TTTCGGAATAATAGGCTTGGAAATCCTCCCCTTCCACGAAATCAAGTGGGCACCATTTCTGCTGGAAAGC
  CAATGTTTTCTCATCAAGTGCCCCAGAAAGTGAAATATCCACCACCATTCCCAGTGGGACCCAACTCATC
  TCTTCTCTTCTCCTCCCATGCTTTGGGGGAATCCCATGCTTTTTCTGAGGATCCCATGCTGCAGAACAGC
  CCCTTTGCCAATTGGGCTGTCTCCTATGACTCTTCTGCATCCCAGTTTCCCAATTACCTGCCTTCTAAAG
  CCTCACCTCCTTTGGGACCAGACTCTTCCCACTCCTCTTCCTCTGATGGTGATGAGCCAAATGGAGCTAG
  CTCTGATCATATCACAGAAGCATTTCATCACCAGCCTGAGTGGGGAAATCCCAATCGTGACAGAGGGTCC
  TGGGCACAGCCTGTTGATACTGGAGTTTCAGAAGCGAGCCTAGGTGATGGTGAGCCCCACATCCCATCTC
  TGCTGTCTATGTCTACAAGGAACCACATGGATATCACCATTCCACCCTTACCTCCAGTAGCTCCAGAAGT
  CTTGAGAGTTGCTGAACACAGACACCGGAGGGGTCTTATGTACCCATATATCTACCATGTCCTCACTAAG
  GGTGAAATTAAGATCCCCGTATGTATTGAGGATGAGTGTAACATGGAGCTGCCTCCAGCTGCTCTCTTAT
  TCCGGTCAGCTCGTCAATATGTATATGGAGTTCTTTTTAGTCTGGCAGAGACACAGAGGAAAATGGAACG
  CTTGGCCATGCGACGGCGGCTGCCTGTGGAAGTTCCTTCAGTGATCCTTAAAGAGTGGTCTGCCTATAAA
  GGGAAGTCACCTCAAACCCCTGAGCTGGTGTCTGCACTGACATTTCGGGAATGGACTTGCCCAAACCTCA
  AGAAGCTCTGGCTAGGCAAAGCAGTTGAAGACAAGAACAGAAGGATGCGGGCCTTCCTGGCCTGTATGAA
  GTCGGACACGCCCAGTATGCTCAATCCAGCTAATGTCCCCACCCATCTGCTGCTCATGTGTTGTGTACTC
  CGGTACATGGTTCAGTGGCCTGGTGGCCGAATCCTGCATCGCCATGAGCTAGACACCTTCCTTGCACAGG
  CAGTGTCTACCCAGCTTTATGAACCAGATCGACTCCAAGAACTCAAGGTCTCCATCCAATCCCACCCCAA
  GGAGGAAAACTGGAGATTGCTGGGATGGTTGTGGGCCAGTGGGCTGGCAGCAGATCCTCCAGGGGCCGAG
  GATCCTTCGGCATGCAAGTGGTTTCTGTCGGTGGGCCAGGAAAGGGGCATGGAAAAGAACAGACTGGTAG
  AGGATCCAAGGGACACAAAAAAGGAAATAAGCAAGGCTCTTCAGATGGAGTTTCTAAATCCCTGGAGCTT
  CATCAAGGTCGGTCTCGCTCCCAGGTAA
  
  
• Restriction Sites: SgfI-MluI
• ACCN: NM_001300788
• ORF Size: 2688 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_001300788.1, NP_001287717.1
• RefSeq Size: 7678
• RefSeq ORF: 2688
• Locus ID: 54954
• Gene Summary: This gene encodes a potential transmembrane protein and lies in a region where mutations and deletions have been associated with intellectual disability and autism. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2011]
  Transcript Variant: This variant (3) lacks two exons in the 3' coding region which results in a frameshift compared to variant 1. The encoded isoform (3) is shorter than and has a distinct C-terminus compared to isoform 1. Sequence Note: This RefSeq record was created from transcript and genomic sequence data to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on transcript alignments.