Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Summary ExpressionExpr. PhenotypesPheno. Gene Literature (218)Lit. (218) GO Terms (20)GO (20) Nucleotides (143)Nucl. (143) Proteins (43)Prot. (43) Interactants (774)Interact. (774) Wiki
XB-GENEPAGE-1011225
???displayGene.symbol???:
 mmut

???displayGene.name???: 
methylmalonyl-CoA mutase

???displayGene.synonyms???
mcm , mut ( Nomenclature history )

AI Protein Function :
mmut encodes a mitochondrial enzyme that catalyzes the isomerization of methylmalonyl‑CoA to succinyl‑CoA, a key step in the catabolism of propionate and branched‑chain amino acids. The protein is loca...[+]


InterPro :
Acid CoA mut C, Cbl-dep enz cat, Cobalamin-bd, Cobalamin-bd sf, [+]

???displayGene.geneInteractants???
Loading ...

Diseases: 


Disease Ontology:
methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency

MIM:
METHYLMALONIC ACIDURIA DUE TO METHYLMALONYL-CoA MUTASE DEFICIENCY; MAMM

External Links:
Loading gene data...
Please wait while we fetch the latest information
???displayGene.expression???                  Development Stages                                               Embryonic Tissues                                                                Adult Tissues
More Information
Xenbase Expression Details In situ images Single cell data at SPRING In situ: RNA-Seq:


Symbol legend: Blast sequence    View sequence    Literature or expression images   Hover cursor for info