DFNB31 (WHRN) (NM_015404) Human Untagged Clone

CAT#: SC304310

DFNB31 (untagged)-Human deafness, autosomal recessive 31 (DFNB31), transcript variant 1

Specifications

Product Data

• Type: Human Untagged Clone
• Tag: Tag Free
• Symbol: WHRN
• Synonyms: CIP98; DFNB31; PDZD7B; USH2D; WI
• Vector: pCMV6-Entry
• E. coli Selection: Kanamycin (25 ug/mL)
• Mammalian Cell Selection: Neomycin
• Sequence Data:
  Fully Sequenced ORF

  >NCBI ORF sequence for NM_015404, the custom clone sequence may differ by one or more nucleotides
  
  
  ATGAACGCGCCGCTGGACGGCCTGTCGGTGAGCTCGTCCTCCACCGGCTCGCTGGGCTCGGCGGCCGGGG
  CGGGCGGCGGCGGGGGCGCGGGGCTGCGGTTACTGTCTGCCAACGTGCGCCAGCTGCACCAAGCGCTGAC
  CGCGCTGCTGAGCGAGGCGGAGCGGGAGCAGTTCACCCACTGCCTGAACGCTTACCACGCGCGCCGCAAC
  GTCTTCGACCTGGTGCGCACCCTGCGCGTGCTGCTGGACAGTCCGGTCAAGCGGCGCCTGCTGCCCATGC
  TTCGTCTGGTCATCCCGCGCTCCGACCAGCTGCTCTTCGACCAATACACGGCCGAGGGCCTCTACCTGCC
  CGCCACCACCCCCTACAGGCAGCCCGCCTGGGGCGGCCCCGACAGCGCGGGGCCAGGGGAGGTGCGCCTG
  GTGAGTTTGCGGCGTGCCAAGGCCCACGAGGGCTTGGGCTTCAGCATCCGTGGGGGCTCGGAGCACGGCG
  TGGGCATCTACGTGTCTCTGGTGGAACCAGGCTCTCTAGCTGAGAAGGAAGGACTGCGGGTCGGGGACCA
  GATTCTGCGCGTCAACGACAAATCCCTGGCCCGGGTGACCCACGCGGAGGCCGTCAAGGCTCTGAAGGGC
  TCCAAGAAGCTGGTGCTGTCTGTGTACTCAGCAGGGCGCATCCCTGGGGGCTACGTCACCAACCACATCT
  ACACCTGGGTGGACCCGCAGGGCCGCAGCATCTCCCCACCCTCGGGCCTGCCCCAGCCCCACGGTGGTGC
  CCTGAGGCAGCAGGAGGGTGACCGGAGGAGCACCCTGCACCTCCTGCAAGGAGGGGATGAGAAAAAGGTG
  AACCTGGTGCTGGGGGACGGCCGGTCCCTGGGCCTCACGATCCGTGGGGGAGCTGAGTACGGCCTTGGCA
  TTTACATCACTGGCGTGGACCCAGGCTCTGAAGCAGAAGGCAGCGGGCTCAAGGTTGGGGACCAGATTCT
  AGAAGTGAATGGGCGGAGCTTTCTCAACATCCTACACGACGAGGCTGTCAGGCTGCTTAAGTCATCTCGG
  CACCTCATCCTGACAGTGAAGGACGTCGGGAGGCTGCCCCATGCCCGCACCACTGTGGACGAGACCAAGT
  GGATCGCCAGTTCCCGGATCAGGGAGACCATGGCGAACTCGGCAGGGTTTCTTGGCGATCTCACAACAGA
  AGGAATAAACAAGCCAGGATTTTACAAGGGCCCAGCCGGCTCCCAGGTGACCCTGAGCAGCCTGGGGAAC
  CAGACACGAGTGCTGCTGGAGGAGCAGGCTCGGCACCTGCTGAACGAGCAGGAACACGCCACCATGGCCT
  ACTACCTGGATGAGTACCGTGGTGGCAGCGTCTCTGTGGAGGCCCTCGTCATGGCCCTGTTCAAGCTGCT
  CAACACCCACGCCAAGTTCTCACTCCTCTCTGAGGTGAGAGGCACCATTTCCCCGCAAGACCTAGAACGC
  TTCGACCACCTGGTGCTGAGGCGTGAGATTGAGTCCATGAAGGCGCGGCAGCCCCCAGGCCCCGGGGCTG
  GGGACACCTACTCCATGGTCTCCTACAGTGACACGGGTTCATCCACAGGCAGCCACGGCACCTCCACCAC
  CGTCAGCTCGGCCAGGAACACTCTGGACCTGGAGGAAACTGGCGAGGCTGTCCAGGGCAATATCAACGCC
  CTCCCAGATGTGTCCGTGGATGATGTCAGATCCACCTCCCAGGGGCTGTCAAGCTTCAAGCCACTGCCTC
  GCCCACCACCTCTGGCCCAAGGCAACGACCTCCCACTAGGCCAGCCAAGGAAGCTGGGGAGAGAGGACCT
  CCAGCCACCTTCCTCCATGCCTTCCTGCTCGGGCACTGTCTTCTCGGCTCCACAGAACCGCAGCCCGCCA
  GCGGGCACCGCACCCACCCCAGGGACCTCCTCTGCACAGGACTTGCCCTCTTCCCCCATCTATGCCTCCG
  TCTCCCCTGCCAACCCCAGCTCCAAGAGGCCGCTGGACGCCCATCTGGCCCTGGTCAACCAACACCCCAT
  CGGCCCCTTCCCACGGGTCCAGTCACCCCCGCACCTGAAAAGCCCCTCTGCAGAGGCCACAGTGGCTGGG
  GGCTGCCTTCTGCCCCCATCACCCTCTGGCCACCCAGACCAGACAGGCACAAACCAGCACTTTGTCATGG
  TGGAGGTCCACCGCCCCGACAGCGAGCCAGACGTCAATGAAGTGAGGGCGCTGCCCCAGACGCGCACAGC
  CTCTACGCTCTCCCAGCTCTCGGACAGCGGGCAGACTCTAAGCGAGGACAGTGGTGTGGATGCTGGCGAG
  GCAGAGGCCAGCGCCCCAGGCCGAGGAAGGCAGTCGGTGTCCACCAAGAGCAGGAGTAGCAAGGAGCTGC
  CTCGGAACGAGAGGCCCACAGATGGGGCCAACAAACCGCCTGGACTTCTGGAGCCCACGTCCACTCTGGT
  CCGTGTGAAGAAAAGTGCGGCCACCCTGGGCATCGCCATCGAGGGTGGCGCCAACACCCGCCAGCCCCTG
  CCTAGGATTGTCACTATTCAGAGAGGCGGCTCAGCTCACAACTGTGGGCAGCTCAAGGTGGGCCACGTGA
  TTCTGGAAGTGAATGGGCTGACGCTTCGGGGCAAGGAGCACCGGGAGGCCGCCCGCATTATCGCCGAGGC
  CTTCAAGACTAAGGACCGTGACTACATTGACTTTCTGGTCACTGAGTTCAATGTGATGCTCTAG
  
  
• Restriction Sites: SgfI-MluI
• ACCN: NM_015404
• ORF Size: 2724 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).
• OTI Annotation: This TrueClone is provided through our Custom Cloning Process that includes sub-cloning into OriGene's pCMV6 vector and full sequencing to provide a non-variant match to the expected reference without frameshifts, and is delivered as lyophilized plasmid DNA.

Reference Data

• RefSeq: NM_015404.3, NP_056219.3
• RefSeq Size: 4079
• RefSeq ORF: 2724
• Locus ID: 25861
• Gene Summary: This gene is thought to function in the organization and stabilization of sterocilia elongation and actin cystoskeletal assembly, based on studies of the related mouse gene. Mutations in this gene have been associated with autosomal recessive non-syndromic deafness and Usher Syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2016]
  Transcript Variant: This variant (1) represents the longest transcript and encodes the longest isoform (1).