Mmut methylmalonyl-Coenzyme A mutase [ Mus musculus (house mouse) ] - Gene - Data resources

17850

Mmut methylmalonyl-Coenzyme A mutase [ Mus musculus (house mouse) ]
Source: NCBI Gene (ID 17850)

Symbol: Mmut

Full name: methylmalonyl-Coenzyme A mutase

Gene type: protein coding

RefSeq status: VALIDATED

Also known as: D230010K02Rik; Mcm; Mut

Summary: Enables methylmalonyl-CoA mutase activity. Acts upstream of or within post-embryonic development. Located in mitochondrion. Is expressed in several structures, including alimentary system; genitourinary system; lung; nervous system; and trophectoderm. Used to study methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency. Human ortholog(s) of this gene implicated in methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency. Orthologous to human MMUT (methylmalonyl-CoA mutase). [provided by Alliance of Genome Resources, Apr 2022]

Expression: Ubiquitous expression in kidney adult (RPKM 18.8), liver E18 (RPKM 12.2) and 24 other tissues

Orthologs: human

Gene size: 27305bp

Exon count: 14