SHFM1 (NM_006304) Human Untagged Clone

CAT#: SC111062

SHFM1 (untagged)-Human split hand/foot malformation (ectrodactyly) type 1 (SHFM1)

Specifications

Product Data

• Type: Human Untagged Clone
• Tag: Tag Free
• Symbol: SHFM1
• Synonyms: C7orf76; DSS1; ECD; SHFD1; Shfdg1; SHFM1; SHSF1
• Vector: pCMV6-XL5
• E. coli Selection: Ampicillin (100 ug/mL)
• Mammalian Cell Selection: None
• Sequence Data:
  Fully Sequenced ORF

  >OriGene ORF within SC111062 sequence for NM_006304 edited (data generated by NextGen Sequencing)
  ATGTCAGAGAAAAAGCAGCCGGTAGACTTAGGTCTGTTAGAGGAAGACGACGAGTTTGAA
  GAGTTCCCTGCCGAAGACTGGGCTGGCTTAGATGAAGATGAAGATGCACATGTCTGGGAG
  GATAATTGGGATGATGACAATGTAGAGGATGACTTCTCTAATCAGTTACGAGCTGAACTA
  GAGAAACATGGTTATAAGATGGAGACTTCATAG
  
  Clone variation with respect to NM_006304.1
  
  5' Read Nucleotide Sequence

  >OriGene 5' read for NM_006304 unedited
  TGGGGGTTCGNATTTTGTAATACGACTCACTATAGGGCGGCNCGCGATTCGGCACGAGGG
  AGGGTTCCAACTTTTCTGCTTATCTGGGAGGTGTTGGGCGCGGACAGTCGAGATGTCAGA
  GAAAAAGCAGCCGGTAGACTTAGGTCTGTTAGAGGAAGACGACGAGTTTGAAGAGTTCCC
  TGCCGAAGACTGGGCTGGCTTAGATGAAGATGAAGATGCACATGTCTGGGAGGATAATTG
  GGATGATGACAATGTAGAGGATGACTTCTCTAATCAGTTACGAGCTGAACTAGAGAAACA
  TGGTTATAAGATGGAGACTTCATAGCATCCAGAAGAAGTGTTGAAGTAACCTAAACTTGA
  CCTGCTTAATACATTCTAGGGCAGAGAACCCAGGATGGGACACTAAAAAAATGTGTTTAT
  TTCATTATCTGCTTGGATTTATTTGTGTTTTTGTAACACAAAAAATAAATGTTTTGATAT
  AATCTTGGTTTGGTTCAGACCACACACACCACCCCCCCCCCCCCCCCCACCCACCCACCC
  AAAAAAACTCGACTCTAGATTGCGGCCGCGGCCATAGCTGTTTCCTGAACAGATCCCGGG
  TGGCATCCCTGTGACCCCTCCCCAGTGCCTTTCCTGGCCCTGGAAGTTGCCACTCCAGTG
  CCCACCAGCCTTGTCCTAATAAAATTAAGTTGCATCATTTTGTCTGACTAGGGGTCCTTC
  TATATATTATGGGGTGGGGGGGGGGCGTTGGAGCCAGGGGCCATTTGGGAAAACACCCGC
  ACGGCCCTCGGGGCCTTATTGGACCCAACCGGAACCGCCGGCCCATCCTGGCTCCTGCAT
  TCCCCCCCCCCGGGTCCAAGCCATTTCCCTGCCCCACCT
  
  3' Read Nucleotide Sequence

  >OriGene 3' read for NM_006304 unedited
  ATGGACGCGGCCGCAATCTAGGATCGAGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
  TTTTTTTTTTTTTTTTTCGGAACCAAACCAAAATTATTTCAAAACATTTATTTTTTGGGT
  TACAAAAACACAAATAAATCCAAGCAGATAATGAAATAAACACATTTTTTTAGGGGCCCA
  TCCTGGGTTCTCTGCCCTAAAATGTATTAAGCAGGTCAAGTTTAGGTTACTTCAACACTT
  TTTTTGGATGCTATGAAGTCTCCATTTTATAACCATGTTTCTTTAGTTCAGCTCGAAACT
  GATTAAAAAAGTCATCCTTTACATTGGCATCATCCCAATTATCCTCCCAAACATGGGCAT
  TTTCATTTTCATCTAAGCCAGCCCAGTCTTCGGGAGGGAACTTTTAAAACTCGTCGTTTT
  CCTTTAACAAACCTAAGTCTACCGGCTGGTTTTTTTTTGACATTTGGACTGGCCGCGCCC
  AACACCTCCCAAATAAGCAAAAAAGTTGGAACCCTCCCTCGTGCCGAATTCGCGGCCGCC
  CTATAGGGAGTCGTATTACAAAATTCTGACGGTTCACTAAACGAGCTCTGCTTATATAAA
  CCTCCCACCGTACACGCCTACCGCCCATTTGGGTCAACGGGGCGGGGTTATTACCACATT
  TTGGAAAGTCCCGTTGATTTTGGTGCCAAAACAAACTCCCATTGACGTCAATGGGGTGGG
  AAACTTGGAAATCCCCGTGAGTCAAACCGCTATCCACGCCCATTGTTGTACTGCCAAAAC
  CGCATCACCATGGTAATAGCGATGACTAAACNTANATGTACTGCCAAGTAGAAAGTCCCG
  TAGGTCATGTACTGGCATAAATGCAGCGGGCCATTTACCGCANTGACGTCAATAGGGGCG
  ACTNGCATAAGAACCTGGATGC
  
• Restriction Sites: NotI-NotI
• ACCN: NM_006304
• ORF Size: 213 bp
• Insert Size: 520
• 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_006304.1, NP_006295.1
• RefSeq Size: 509
• RefSeq ORF: 213
• Locus ID: 7979
• Domains: DSS1_SEM1
• Protein Pathways: Homologous recombination, Proteasome
• Gene Summary: The product of this gene has been localized within the split hand/split foot malformation locus SHFM1 at chromosome 7. It has been proposed to be a candidate gene for the autosomal dominant form of the heterogeneous limb developmental disorder split hand/split foot malformation type 1. In addition, it has been shown to directly interact with BRCA2. It also may play a role in the completion of the cell cycle. [provided by RefSeq, Jul 2008]
  Transcript Variant: This variant (5) differs in the 3' exon structure and the entire coding region, compared to variant 1. It encodes isoform 3, which has a completely different sequence, compared to isoform 1.