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Publication : Mapping of human methylmalonyl CoA mutase (MUT) locus on chromosome 6.

First Author  Ledley FD Year  1988
Journal  Am J Hum Genet Volume  42
Issue  6 Pages  839-46
PubMed ID  2897160 Mgi Jnum  J:23659
Mgi Id  MGI:71534 Citation  Ledley FD, et al. (1988) Mapping of human methylmalonyl CoA mutase (MUT) locus on chromosome 6. Am J Hum Genet 42(6):839-46
abstractText  Methylmalonyl CoA mutase (MCM) catalyzes an essential step in the degradation of several branch-chain amino acids and odd-chain fatty acids. Deficiency of this apoenzyme causes the mut form of methylmalonic acidemia, an often fatal disorder of organic acid metabolism. An MCM cDNA has recently been obtained from human liver cDNA libraries. This clone has been used as a probe to determine the chromosomal location of the MCM gene and MUT locus. Southern blot analysis of DNA from human-hamster somatic-cell hybrid cell lines assigned the locus to region q12-p23 of chromosome 6. In situ hybridization further localized the locus to the region 6p12-21.2. A highly informative RFLP was identified at the MCM gene locus which will be useful for genetic diagnostic and linkage studies.
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