FLCN (NM_144997) Human Untagged Clone

CAT#: SC127885

FLCN (untagged)-Human folliculin (FLCN), transcript variant 1

Specifications

Product Data

• Type: Human Untagged Clone
• Tag: Tag Free
• Symbol: FLCN
• Synonyms: BHD; DENND8B; FLCL
• Vector: pCMV6-XL4
• E. coli Selection: Ampicillin (100 ug/mL)
• Mammalian Cell Selection: None
• Sequence Data:
  Fully Sequenced ORF

  >OriGene ORF within SC127885 sequence for NM_144997 edited (data generated by NextGen Sequencing)
  ATGAATGCCATCGTGGCTCTCTGCCACTTCTGCGAGCTCCACGGCCCCCGCACTCTCTTC
  TGCACGGAGGTGCTGCACGCCCCACTTCCTCAAGGGGATGGGAATGAGGACAGTCCTGGC
  CAGGGTGAGCAGGCGGAAGAAGAGGAAGGTGGCATTCAGATGAACAGTCGGATGCGTGCG
  CACAGCCCCGCAGAGGGGGCCAGCGTCGAGTCCAGCAGCCCGGGGCCCAAAAAGTCGGAC
  ATGTGCGAGGGCTGCCGGTCACTTGCTGCAGGGCACCCGGGATATATCAGCCATGATAAA
  GAGACCTCCATTAAATACGTCAGCCACCAGCACCCCAGCCACCCCCAGCTCTTCAGCATT
  GTCCGCCAGGCCTGTGTCCGGAGCCTGAGCTGTGAGGTCTGCCCTGGCCGTGAAGGCCCC
  ATCTTCTTCGGAGATGAGCAGCACGGCTTTGTGTTCAGCCACACCTTCTTCATCAAGGAC
  AGCCTGGCCAGGGGCTTCCAGCGCTGGTACAGCATCATCACCATCATGATGGACCGGATC
  TACCTCATCAACTCCTGGCCCTTCCTGCTGGGGAAGGTCCGGGGAATCATCGATGAGCTC
  CAGGGCAAGGCGCTCAAGGTGTTTGAGGCAGAGCAGTTTGGATGCCCACAGCGTGCTCAG
  AGGATGAACACAGCCTTCACGCCATTCCTACACCAGAGGAACGGCAACGCCGCCCGCTCG
  CTGACATCGCTGACAAGTGATGACAACCTGTGGGCGTGCCTGCACACCTCCTTTGCCTGG
  CTCCTGAAGGCGTGTGGCAGCCGGCTGACCGAGAAGCTCCTGGAAGGTGCTCCGACCGAG
  GATACCTTGGTCCAGATGGAGAAGCTCGCTGATTTAGAAGAGGAATCAGAAAGCTGGGAC
  AACTCTGAGGCTGAAGAGGAGGAGAAAGCCCCTGTGTTGCCAGAGAGTACAGAAGGGCGG
  GAGCTGACCCAGGGCCCGGCAGAGTCCTCCTCTCTCTCAGGCTGTGGGAGCTGGCAGCCC
  CGGAAGCTGCCAGTCTTCAAGTCCCTCCGGCACATGAGGCAGGTCCTGGGTGCCCCTTCT
  TTCCGCATGCTGGCCTGGCACGTTCTCATGGGGAACCAGGTGATCTGGAAAAGCAGAGAC
  GTGGACCTCGTCCAGTCAGCTTTTGAAGTACTTCGGACCATGCTTCCCGTGGGCTGCGTC
  CGCATCATCCCATACAGCAGCCAGTACGAGGAGGCCTATCGGTGCAACTTCCTGGGGCTC
  AGCCCGCACGTGCAGATCCCCCCCCACGTGCTCTCCTCAGAGTTTGCTGTCATCGTGGAG
  GTCCACGCAGCCGCACGTTCCACCCTCCACCCTGTGGGGTGTGAGGATGACCAGTCTCTC
  AGCAAGTACGAGTTTGTGGTGACCAGTGGGAGCCCTGTAGCTGCAGACCGAGTGGGCCCC
  ACCATCCTGAATAAGATTGAAGCGGCTCTGACCAACCAGAACCTGTCTGTGGATGTGGTG
  GACCAGTGCCTCGTCTGCCTCAAGGAGGAGTGGATGAACAAAGTGAAGGTGCTTTTTAAG
  TTCACCAAGGTGGACAGTCGACCCAAAGAGGACACACAGAAGCTGCTGAGCATCCTGGGT
  GCGTCCGAGGAGGACAATGTCAAGCTGCTGAAGTTCTGGATGACTGGCCTGAGCAAGACC
  TACAAGTCACACCTCATGTCCACGGTCCGCAGCCCCACAGCCTCGGAGTCTCGGAACTGA
  
  Clone variation with respect to NM_144997.5
  
  5' Read Nucleotide Sequence

  >OriGene 5' read for NM_144997 unedited
  GCATTTTGTAATACGACTCACTATAGGGCGGCCGCGAATTCGGCACGAGGGGTCGCTCCT
  GGTTCTGCCAGCTCCCCTGAGAGCCTGAACCCGGGCTTGAGAGCCTCGCCACCCCGGGTG
  ACATCCCTGCCGTGGGCTTGGGGGCTCTGGGTGTGATTCCGCCGGTCCGGGTCCCGCAGC
  GACCACCTACCCAGCGCAGTCAGGGGTGGGGCTGGGACCCAGAGCGGGACCCCGGCTGCC
  GAGTCCAGGTGTCCCGCGGGCCTCGATTTGGGGAGCAGAAAACGCCAGGTCTTCAGAGGG
  TGTCTGCCACCACCATGCCTGACCCATTTGGCAGCAGCCTCGTGTGTGGTGGTCTGGTGT
  GGACGGTGGAAGCGTGATTCTGCTGANTGTCAATGAGACCACTTCTGGCTTAACCCGGTA
  TTCTCAACCGGGAGGGAACAAGTTGCCCGGGAACCAACCTCCGTGGCAAGCTTAAAGCAA
  CCCCAAAACTTGTTGCGGAAAACGTTCAGGGGCCTTGTTTGCAATCCTTCCCAAGGCCAC
  CCATGGGAATGCCCATTCCGTGGGCTTTTTTTTGGCCAATTTTTCTGGGAAAAGCTTTCC
  AAGGGGCCCCCCCCGGAAATTTTTTTTTTCTTTGCACCGGGAAGGTTGCTCTGGAAAGGC
  CCCCAAAATTTTCCTTAAAAGAGGGGATTGGGGAAATTTAAAGGCCAAATCCCCTGGGGC
  CAAGGGGGGTTAAACCAAGGCCCGGAAAAAAAAAAAGGAAAGAGGTGGGGCATTTCCA
  
  3' Read Nucleotide Sequence

  >OriGene 3' read for NM_144997 unedited
  GAGAGGCACTGGGGAGGGGTCACAGGGATGCCACCCGGGATCTGTTCAGGAAACAGCTAT
  GACCGCGGCCGCAATCTAGAGTCGAG
  
• Restriction Sites: Please inquire
• ACCN: NM_144997
• ORF Size: 1740 bp
• Insert Size: 3700
• 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_144997.4, NP_659434.2
• RefSeq Size: 3717
• RefSeq ORF: 1740
• Locus ID: 201163
• Protein Families: Druggable Genome
• Protein Pathways: Renal cell carcinoma
• Gene Summary: This gene is located within the Smith-Magenis syndrome region on chromosome 17. Mutations in this gene are associated with Birt-Hogg-Dube syndrome, which is characterized by fibrofolliculomas, renal tumors, lung cysts, and pneumothorax. Alternative splicing of this gene results in two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]
  Transcript Variant: This variant (1) encodes isoform 1.