Mapping of the l-methylmalonyl-CoA mutase gene to mouse chromosome 17

Jadranka Sertić, Vladimir Vincek, Fred D. Ledley, Felipe Figueroa, Jan Klein

Research output: Contribution to journalArticle

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Abstract

In humans, methylmalonyl acidemia is caused by a deficiency of l-methylmalonyl-CoA mutase (MUT) controlled by a gene that has been mapped to chromosome 6. The mouse homolog of this gene has now been mapped to mouse chromosome 17. Recombinant inbred and congenic strains place the mouse Mut locus 1.06 cM distal to H-2, between Pgk-2 and Ce-2. The relative order of syntenic probes flanking H-2 on mouse chromosome 17 and HLA on human chromosome 6 is shown to be different.

Original languageEnglish (US)
Pages (from-to)560-564
Number of pages5
JournalGenomics
Volume6
Issue number3
DOIs
StatePublished - Mar 1990

All Science Journal Classification (ASJC) codes

  • Genetics

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    Sertić, J., Vincek, V., Ledley, F. D., Figueroa, F., & Klein, J. (1990). Mapping of the l-methylmalonyl-CoA mutase gene to mouse chromosome 17. Genomics, 6(3), 560-564. https://doi.org/10.1016/0888-7543(90)90487-F