KCT2 Proteins, cDNA Clones Research Reagents

C5orf15 (Chromosome 5 Open Reading Frame 15, also known as KCT2; HTGN29), located on 5q31.1, is a Protein Coding gene. The gene produces a 29235 Da protein composed of 265 amino acids. C5orf15 is a single-pass type I membrane protein that is widely expressed in the thyroid, kidney, and other tissues. Diseases such as Arrhythmogenic Right Ventricular Dysplasia, Familial, 5, and Amyotrophic Lateral Sclerosis 11 are associated with C5orf15.

KCT2 Protein (1)

    KCT2 cDNA Clone (13)

    BC020875

    クローニングベクター cDNA 製品

    In lentiviral vector

    KCT2 qPCR Primer (1)

    KCT2 Lysate (1)

      KCT2 の背景知識

      C5orf15 (Chromosome 5 Open Reading Frame 15, also known as KCT2) is a Protein Coding gene. KCT2 gene maps to human chromosome 5q31.1 and is conserved in human, chimpanzee, cow, rat, and chicken. KCT2 is a 265 amino acid single-pass type I membrane protein that is widely expressed in the thyroid, kidney, and other tissues. Chromosome 5 is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Chromosome 5 contains 181 million base pairs and comprises nearly 6% of the human genome. Diseases associated with C5orf15 include Arrhythmogenic Right Ventricular Dysplasia, Familial, 5, and Amyotrophic Lateral Sclerosis 11.

      KCT2 の参考文献

      • Bonkobara M., et al.,(2003), Identification of novel genes for secreted and membrane-anchored proteins in human keratinocytes. Br. J. Dermatol. 148:654-664.
      • Yu W, et al., (1997), Large-scale concatenation cDNA sequencing. Genome Res. 7(4):353-8.
      • Ota T., et al.,(2004), Complete sequencing and characterization of 21,243 full-length human cDNAs.Nat. Genet. 36:40-45.

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