DFNB31 (WHRN) (NM_001173425) Human Untagged Clone

CAT#: SC329217

DFNB31 (untagged)-Human deafness autosomal recessive 31 (DFNB31) transcript variant 3

Specifications

Product Data

• Type: Human Untagged Clone
• Tag: Tag Free
• Symbol: WHRN
• Synonyms: CIP98; DFNB31; PDZD7B; USH2D; WI
• Vector: pCMV6-XL5
• E. coli Selection: Ampicillin (100 ug/mL)
• Mammalian Cell Selection: None
• Sequence Data:
  Fully Sequenced ORF

  >NCBI ORF sequence for NM_001173425, the custom clone sequence may differ by one or more nucleotides
  ATGAACGCGCCGCTGGACGGCCTGTCGGTGAGCTCGTCCTCCACCGGCTCGCTGGGCTCG
  GCGGCCGGGGCGGGCGGCGGCGGGGGCGCGGGGCTGCGGTTACTGTCTGCCAACGTGCGC
  CAGCTGCACCAAGCGCTGACCGCGCTGCTGAGCGAGGCGGAGCGGGAGCAGTTCACCCAC
  TGCCTGAACGCTTACCACGCGCGCCGCAACGTCTTCGACCTGGTGCGCACCCTGCGCGTG
  CTGCTGGACAGTCCGGTCAAGCGGCGCCTGCTGCCCATGCTTCGTCTGGTCATCCCGCGC
  TCCGACCAGCTGCTCTTCGACCAATACACGGCCGAGGGCCTCTACCTGCCCGCCACCACC
  CCCTACAGGCAGCCCGCCTGGGGCGGCCCCGACAGCGCGGGGCCAGGGGAGGTGCGCCTG
  GTGAGTTTGCGGCGTGCCAAGGCCCACGAGGGCTTGGGCTTCAGCATCCGTGGGGGCTCG
  GAGCACGGCGTGGGCATCTACGTGTCTCTGGTGGAACCAGGCTCTCTAGCTGAGAAGGAA
  GGACTGCGGGTCGGGGACCAGATTCTGCGCGTCAACGACAAATCCCTGGCCCGGGTGACC
  CACGCGGAGGCCGTCAAGGCTCTGAAGGGCTCCAAGAAGCTGGTGCTGTCTGTGTACTCA
  GCAGGGCGCATCCCTGGGGGCTACGTCACCAACCACATCTACACCTGGGTGGACCCGCAG
  GGCCGCAGCATCTCCCCACCCTCGGGCCTGCCCCAGCCCCACGGTGGTGCCCTGAGGCAG
  CAGGAGGGTGACCGGAGGAGCACCCTGCACCTCCTGCAAGGAGGGGATGAGAAAAAGGTG
  AACCTGGTGCTGGGGGACGGCCGGTCCCTGGGCCTCACGATCCGTGGGGGAGCTGAGTAC
  GGCCTTGGCATTTACATCACTGGCGTGGACCCAGGCTCTGAAGCAGAAGGCAGCGGGCTC
  AAGGTTGGGGACCAGATTCTAGAAGTGAATGGGCGGAGCTTTCTCAACATCCTACACGAC
  GAGGCTGTCAGGCTGCTTAAGTCATCTCGGCACCTCATCCTGACAGTGAAGGACGTCGGG
  AGGCTGCCCCATGCCCGCACCACTGTGGACGAGACCAAGTGGATCGCCAGTTCCCGGATC
  AGGGAGACCATGGCGAACTCGGCAGGGTTTCTTGGCGATCTCACAACAGAAGGAATAAAC
  AAGCCAGGATTTTACAAGGGCCCAGCCGGCTCCCAGGTGACCCTGAGCAGCCTGGGGAAC
  CAGACACGAGTGCTGCTGGAGGAGCAGGCTCGGCACCTGCTGAACGAGCAGGAACACGCC
  ACCATGGCCTACTACCTGGATGAGTACCGTGGTGGCAGCGTCTCTGTGGAGGCCCTCGTC
  ATGGCCCTGTTCAAGCTGCTCAACACCCACGCCAAGTTCTCACTCCTCTCTGAGGTGAGA
  GGCACCATTTCCCCGCAAGACCTAGAACGCTTCGACCACCTGGTGCTGAGGCGTGAGATT
  GAGTCCATGAAGGCGCGGCAGCCCCCAGGCCCCGGGGCTGGGGACACCTACTCCATGGTC
  TCCTACAGTGACACGGGTTCATCCACAGGCAGCCACGGCACCTCCACCACCGTCAGCTCG
  GCCAGGAACACTCTGGACCTGGAGGAAACTGGCGAGGCTGTCCAGGGCAATATCAACGCC
  CTCCCAGATGTGTCCGTGGATGATGTCAGATCCACCTCCCAGGGGCTGTCAAGCTTCAAG
  CCACTGCCTCGCCCACCACCTCTGGCCCAAGGCAACGACCTCCCACTAGGCCAGCCAAGG
  AAGCTGGGGAGAGAGGACCTCCAGCCACCTTCCTCCATGCCTTCCTGCTCGGGCACTGTC
  TTCTCGGCTCCACAGAACCGCAGCCCGCCAGCGGGCACCGCACCCACCCCAGGGACCTCC
  TCTGCACAGGACTTGCCCTCTTCCCCCATCTATGCCTCCGTCTCCCCTGCCAACCCCAGC
  TCCAAGAGGCCGCTGGACGCCCATCTGGCCCTGGTCAACCAACACCCCATCGGCCCCTTC
  CCACGGGTCCAGTCACCCCCGCACCTGAAAAGCCCCTCTGCAGAGGCCACAGTGGCTGGG
  GGCTGCCTTCTGCCCCCATCACCCTCTGGCCACCCAGACCAGACAGGCACAAACCAGCAC
  TTTGTCATGGTGGAGGTCCACCGCCCCGACAGCGAGCCAGACGTCAATGAAGTGAGGGCG
  CTGCCCCAGACGCGCACCTCTACGCTCTCCCAGCTCTCGGACAGCGGGCAGACTCTAAGC
  GAGGACAGTGGTGTGGATGCTGGCGAGGCAGAGGCCAGCGCCCCAGGCCGAGGAAGGCAG
  TCGGTGTCCACCAAGAGCAGGAGTAGCAAGGAGCTGCCTCGGAACGAGAGGCCCACAGAT
  GGGGCCAACAAACCGCCTGGACTTCTGGAGCCCACGTCCACTCTGGTCCGTGTGAAGAAA
  AGTGCGGCCACCCTGGGCATCGCCATCGAGGGTGGCGCCAACACCCGCCAGCCCCTGCCT
  AGGATTGTCACTATTCAGAGAGGCGGCTCAGCTCACAACTGTGGGCAGCTCAAGGTGGGC
  CACGTGATTCTGGAAGTGAATGGGCTGACGCTTCGGGGCAAGGAGCACCGGGAGGCCGCC
  CGCATTATCGCCGAGGCCTTCAAGACTAAGGACCGTGACTACATTGACTTTCTGGTCACT
  GAGTTCAATGTGATGCTCTAG
  
• Restriction Sites: Please inquire
• ACCN: NM_001173425
• ORF Size: 2721 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_001173425.1, NP_001166896.1
• RefSeq Size: 4076
• RefSeq ORF: 2721
• 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 (3) contains an alternate, in-frame splice site in the 3' coding region, compared to variant 1. The encoded protein (isoform 3) is shorter than isoform 1.