Mmut - methylmalonyl-Coenzyme A mutase Gene

Also Known as Mcm; Mut; D230010K02Rik

Species: Mus musculus

Gene Type: protein coding
Gene ID: 17850

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]

Mmut Products (1)

mRNA Protein Name
NM_008650.3 NP_032676.2 methylmalonyl-CoA mutase, mitochondrial precursor

Gene Ontology

  • Molecular Function
  • Biological Process
Molecular Function GO Annotation Evidence References Source
enables methylmalonyl-CoA mutase activity IDA
IDA: Inferred from direct assay
1978672 MGI
Biological Process GO Annotation Evidence References Source
acts upstream of or within post-embryonic development IMP
IMP: Inferred from mutant phenotype
14555645 MGI
involved in succinyl-CoA biosynthetic process IDA
IDA: Inferred from direct assay
7904153 MGI
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern
Protein Preferred Names Protein Names

methylmalonyl-CoA mutase, mitochondrial

  • methylmalonyl-CoA isomerase

Related Agents

  • Pre-clinical Phase

Pre-clinical Phase

Bioactive Molecules (1)
Cat. No. Product Name
Effect
Purity
Rare Diseases
HY-RS08564 MMUT Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Homo sapiens Mmut NCBI NCBI:4594