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Publication : Cloning, structure, and chromosome localization of the mouse glutaryl-CoA dehydrogenase gene.

First Author  Koeller DM Year  1995
Journal  Genomics Volume  28
Issue  3 Pages  508-12
PubMed ID  7490088 Mgi Jnum  J:28406
Mgi Id  MGI:76024 Doi  10.1006/geno.1995.1182
Citation  Koeller DM, et al. (1995) Cloning, structure, and chromosome localization of the mouse glutaryl-CoA dehydrogenase gene. Genomics 28(3):508-12
abstractText  Glutaryl-CoA dehydrogenase (GCDH) is a nuclear-encoded, mitochondrial matrix enzyme. In humans, deficiency of GCDH leads to glutaric acidemia type I, an inherited disorder of amino acid metabolism characterized by a progressive neurodegenerative disease. In this report we describe the cloning and structure of the mouse GCDH (Gcdh) gene and cDNA and its chromosomal localization. The mouse Gcdh cDNA is 1.75 kb long and contains an open reading frame of 438 amino acids. The amino acid sequences of mouse, human, and pig GCDH are highly conserved. The mouse Gcdh gene contains 11 exons and spans 7 kb of genomic DNA. Gcdh was mapped by backcross analysis to mouse chromosome 8 within a region that is homologous to a region of human chromosome 19, where the human gene was previously mapped.
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