GSG1 (NM_001206845) Human Untagged Clone

CAT#: SC329844

GSG1 (untagged) - Homo sapiens germ cell associated 1 (GSG1), transcript variant 7

Specifications

Product Data

• Type: Human Untagged Clone
• Tag: Tag Free
• Symbol: GSG1
• Synonyms: MGC3146; MGC111023
• Vector: pCMV6 series
• Sequence Data:
  Fully Sequenced ORF

  >NCBI ORF sequence for NM_001206845, the custom clone sequence may differ by one or more nucleotides
  
  
  ATGGCCAAGATGGAGCTCTCGAAGGCCTTCTCTGGCCAGCGGACACTCCTATCTGCCATCCTCAGCATGC
  TATCACTCAGCTTCTCCACAACATCCCTGCTCAGCAACTACTGGTTTGTGGGCACACAGAAGGTGCCCAA
  GCCCCTGTGCGAGAAAGGTCTGGCAGCCAAGTGCTTTGACATGCCAGTGTCCCTGGATGGAGATACCAAC
  ACATCCACCCAGGAGGTGGTACAATACAACTGGGAGACTGGGGATGACCGGTTCTCCTTCCGGAGCTTCC
  GGAGTGGCATGTGGCTATCCTGTGAGGAAACTGTGGAAGAACCAGGGGAGAGGTGCCGAAGTTTCATTGA
  ACTTACACCACCAGCCAAGAGAGGTCTCCTGGGGATGGTGGCCCACATGATGTATTCACAAGTCTTCCAA
  GCGACTGTCAACTTGGGTCCAGAAGACTGGAGACCACATGTTTGGAATTATGGCTGGGCCTTCTACATGG
  CCTGGCTCTCCTTCACCTGCTGCATGGCGTCGGCTGTCACCACCTTCAACACGTACACCAGGATGGTGCT
  GGAGTTCAAGTGCAAGCATAGTAAGAGCTTCAAGGAAAACCCGAACTGCCTACCACATCACCATCAGTGT
  TTCCCTCGGCGGCTGTCAAGTGCAGCCCCCACCGTGGGTCCTTTGACCAGCTACCACCAGTATCATAATC
  AGCCCATCCACTCTGTCTCTGAGGGAGTCGACTTCTACTCCGAGCTGCGGAACAAGGGATTTCAAAGAGG
  GGCCAGCCAGGAGCTGAAAGAAGCAGTTAGGTCATCTGTAGAGGAAGAGCAGTGTTAG
  
  
• Restriction Sites: SgfI-MluI
• ACCN: NM_001206845
• ORF Size: 828 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).

Reference Data

• RefSeq: NM_001206845.1, NP_001193774.1
• RefSeq Size: 2391
• RefSeq ORF: 828
• Locus ID: 83445
• Protein Families: Transmembrane
• Gene Summary: May cause the redistribution of PAPOLB from the cytosol to the endoplasmic reticulum. [UniProtKB/Swiss-Prot Function]
  Transcript Variant: This variant (7) uses an alternate splice site and lacks an alternate exon, resulting in a frameshift in the 3' coding region, compared to variant 1. The encoded isoform (7) has a distinct C-terminus and is shorter than isoform 1. Sequence Note: The RefSeq transcript and protein were derived from genomic sequence to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on alignments.