Dclre1c (NM_146114) Mouse Untagged Clone

CAT#: MC220905

Dclre1c (untagged) - Mouse DNA cross-link repair 1C, PSO2 homolog (S. cerevisiae) (Dclre1c), transcript variant 1, (10ug)

Specifications

Product Data

• Type: Mouse Untagged Clone
• Tag: Tag Free
• Symbol: Dclre1c
• Synonyms: 9930121L06Rik; AI661365; Art; Snm1l
• Vector: pCMV6-Entry
• E. coli Selection: Kanamycin (25 ug/mL)
• Mammalian Cell Selection: Neomycin
• Sequence Data:
  Fully Sequenced ORF

  >MC220905 representing NM_146114
  Red=Cloning site Blue=ORF Orange=Stop codon
  
  TTTTGTAATACGACTCACTATAGGGCGGCCGGGAATTCGTCGACTGGATCCGGTACCGAGGAGATCTGCC
  GCCGCGATCGCC
  
  ATGAGCTCCTTCCAGGGACAGATGGCGGAGTATCCAACCATCTCCATTGACCGCTTCGACAGGGAGAACC
  TGAAAGCCCGTGCCTACTTCCTTTCGCACTGTCACAAGGATCACATGAAAGGATTAAGGGCTCCTTCCTT
  GAAAAGAAGGCTGGAATGCAGCTTGAAGGTCTTCCTGTACTGTTCTCCAGTCACTAAGGAGCTGTTGTTA
  ACTAGCCCAAAGTACAGATTCTGGGAAAACAGAATTATAACAATTGAAATTGAAACTCCTACGCAGATAT
  CTTTAGTTGATGAGGCTTCGGGTGAGAAGGAAGAGGTTGTTGTGACTCTCTTACCAGCTGGTCACTGCCC
  AGGATCAGTTATGTTTTTATTTCAGGGCAGTAATGGAACTGTCTTATACACAGGAGACTTCAGACTGGCA
  AAAGGAGAAGCTTCCAGAATGGAGCTTCTGCACTCTGGAGGCAGAGTAAAAGACATCCAAAGTGTGTATT
  TAGACACGACTTTCTGTGACCCAAGGTTTTATCAGATCCCAAGTCGTGAGCAGTGTTTGAGGGGCATTTT
  GGAGCTGGTTCGGAGCTGGGTCACTAGGAGTCCGCACCACGTCGTGTGGCTGAACTGTAAAGCAGCTTAT
  GGCTACGAGTATTTATTCACCAACCTAAGCGAGGAGCTGGGAGTTCAGGTTCATGTGGACAAGCTGGACA
  TGTTTAAAAACATGCCTGATATCCTGCACCATCTCACAACGGACAGAAACACCCAGATCCACGCCTGCCG
  CCACCCAAAGGCAGAAGAGTGTTTTCAGTGGAATAAACTACCCTGTGGTATAACTTCCCAAAACAAAACT
  GCACTCCACACAATCAGCATCAAGCCATCTACCATGTGGTTTGGAGAGAGGACCAGAAAAACCAACGTGA
  TCGTTAGGACTGGAGAGAGCTCATACAGAGCTTGCTTCTCTTTTCACTCCTCCTTCAGTGAGATTAAAGA
  TTTTTTGAGCTACATCTGCCCAGTGAATGTGTATCCAAATGTCATCCCAGTTGGCCTCACTGTGGATAAG
  GTCATGGACGTTTTAAAGCCTCTGTGCCGGTCTCCCCAAAGTGTTGAGCCAAAGTACAAACCGCTTGGAA
  AATTGAAGAGAGCCAGAACAATCCATCTTGACTCGGAGGAAGACGATGATCTCTTTGATGACCCTCTACC
  GACACCTTTAAGGCACAAAGTTCCGTACCAGCTAACTCTTCAGCCTGAGCTGTTTTCAATGAAGGCACTG
  CCACTAGACCAGCCTGAACTGAGACAAAGCCCAGGAGGCTGCAAAGCAGAGAGTGTGTGGAGCCCTTCTT
  TGGCTAACTTCATAGACTGTGAAGAATCCAACAGCGACAGTGGAGAAGAGCTAGAAACCCCACCACCCTC
  ACTGCAGGGAGGTCTGGGCCCCTCGACACTCGTCCAGCAAAATGCTGATCCGGATGTGGACATACCACAG
  TGGGAAGTCTTCTTCAAAAGAAGAGATGAAATCACAGGTGAATGTTTGGAACACTTACCTTCCTCCATAG
  AGACAGGGGGATCTCAGTCACCAAAGCTCTGCAGTGACTCACCAAAGCTCTGCAGTGACTCACCAAAGCT
  CTGCAGTGACTCTGATGGAGACTCCACCCATATCTCTTCCCAGAATTCATCTCAGTCAACCCATATAACA
  GATCAAGGAAGTCAAGGCTGGGACAGCCAGTGTGATACTGTTTTGTTATCTTCCCAAGAGAAAAGTGGTG
  GGGATAGTACCTCTTTAAACAAGGGTGCCTACAAACCAAAACTCAAAGAGAGTATTTCTGCCTCTCAAAT
  AGAACAGGATGCACTGTGTCCACAAGATACTCACTGTGATTTGAAAAGCAGAGCTGAAGTAAATGGAGCC
  CCTTGTCTTGTAGAACTAGACACCCTGAGTGGCAGGAAGTCTCCACCTGAGAAGACATTGCTAAGCAGCA
  CACGTGCAGACTCACAGAGCTCCTCTGACTTTGAAATCCCCTCAACTCCCGAAGCGGAGCTTCCTACGCC
  AGAGCATTTGCAGTGCTTATACAGGAAACTGGCAACAGGTCAAAGTATAGTTGTCGAAAAAAGAAAATGT
  TCACTTTTAGATAGTTAA
  
  ACGCGTACGCGGCCGCTCGAGCAGAAACTCATCTCAGAAGAGGATCTGGCAGCAAATGATATCCTGGATT
  ACAAGGATGACGACGATAAGGTTTAA
• Restriction Sites: SgfI-MluI
• ACCN: NM_146114
• ORF Size: 2118 bp
• Insert Size: 2118
• 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_146114.3, NP_666226.2
• RefSeq Size: 3759
• RefSeq ORF: 2118
• Locus ID: 227525
• Gene Summary: This gene encodes a member of the SNM1 family of nucleases and is involved in V(D)J recombination and DNA repair. This protein has single-strand-specific 5'-3' exonuclease activity; it also exhibits endonuclease activity on 5' and 3' overhangs and hairpins. The protein also functions in the regulation of the cell cycle in response to DNA damage. Homozygous knockout mice for this gene exhibit severe combined immunodeficiency with sensitivity to ionizing radiation. Mutations in this gene in humans can cause Athabascan-type severe combined immunodeficiency (SCIDA) and Omenn syndrome. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Nov 2014]
  Transcript Variant: This variant (1) encodes the longest isoform (1). Sequence Note: This RefSeq record was created from transcript and genomic sequence data because no single transcript was available for the full length of the gene. The extent of this transcript is supported by transcript alignments.