2. Gene
  3. Mmut - methylmalonyl-CoA mutase Gene

Mmut - methylmalonyl-CoA mutase Gene

  • Gene
  • Protein
  • Agent
  • Ortholog
Rattus norvegicus

Also known as Mut

Gene ID: 688517 | Gene type: protein coding

About Mmut

Summary

Predicted to enable several functions, including cobalamin binding activity; methylmalonyl-CoA mutase activity; and protein homodimerization activity. Predicted to be involved in homocysteine metabolic process and positive regulation of GTPase activity. Predicted to act upstream of or within post-embryonic development. Predicted to be located in mitochondrial matrix. Predicted to be active in mitochondrion. 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_001399409.1 NP_001386338.1 methylmalonyl-CoA mutase
Protein Preferred Names Protein Names

methylmalonyl-CoA mutase

methylmalonyl-CoA mutase, mitochondrial

methylmalonyl-Coenzyme A mutase

rCG43751-like

Related Agents

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