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The human ATP binding cassette gene ABCA13, located on chromosome 7p12.3, encodes a 5058 amino acid protein with an extracellular domain encoded in part by a 4.8-kb conserved exon

  1. Author:
    Prades, C.
    Arnould, I.
    Annilo, T.
    Shulenin, S.
    Chen, Z. Q.
    Orosco, L.
    Triunfol, M.
    Devaud, C.
    Maintoux-Larois, C.
    Lafargue, C.
    Lemoine, C.
    Denefle, P.
    Rosier, M.
    Dean, M.
  2. Author Address

    NCI Frederick, Human Genet Sect, Lab Genom Divers, Bld 560,Rm 21-18, Frederick, MD 21702 USA NCI Frederick, Human Genet Sect, Lab Genom Divers, Frederick, MD 21702 USA NCI Frederick, Intramural Res & Support Program, SAIC Frederick, Frederick, MD 21702 USA Aventis Pharma SA, Funct Genom, Vitry Sur Seine, France Ist Pediat, Mexico City, DF, Mexico Aventis Pharmaceut, Evry, France Dean M NCI Frederick, Human Genet Sect, Lab Genom Divers, Bld 560,Rm 21-18, Frederick, MD 21702 USA
    1. Year: 2002
  1. Journal: Cytogenetic and Genome Research
    1. 98
    2. 2-3
    3. Pages: 160-168
  2. Type of Article: Article
  1. Abstract:

    The ABCA subfamily of ATP-binding cassette (ABC) transporters includes eleven members to date. In this study, we describe a new, unusually large gene on chromosome 7p12.3, ABCA13. This gene spans over 450 kb and is split into 62 exons. The predicted ABCA13 protein consists of 5,058 amino acid residues making it the largest ABC protein described to date. Like the other ABCA subfamily members, ABCA13 contains a hydrophobic, predicted transmembrane segment at the N-terminus, followed by a large hydrophilic region. In the case of ABCA13, the hydrophilic region is unexpectedly large, more than 3,500 amino acids, encoded by 30 exons, two of which are 4.8 and 1.7 kb in length. These two large exons are adjacent to each other and are conserved in the mouse Abca13 gene. Tissue profiling of the major transcript reveals the highest expression in human trachea, testis, and bone marrow. The expression of the gene was also determined in 60 tumor cell lines and the highest expression was detected in the SR leukemia, SNB-19 CNS tumor and DU-145 prostate tumor cell lines. ABCA13 has high similarity with other ABCA subfamily genes which are associated with human inherited diseases: ABCA 1 with the cholesterol transport disorders Tangier disease and familial hypoalphalipoproteinemia, and ABCA4 with several retinal degeneration disorders. The ABCA 13 gene maps to chromosome 7p12.3, a region that contains an inherited disorder affecting the pancreas (Shwachman-Diamond syndrome) as well as a locus involved in T-cell tumor invasion and metastasis (INM7), and therefore is a positional candidate for these pathologies. Copyright (C) 2002 S. Karger AG, Basel.

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