2. Gene
  3. Mmaa - metabolism of cobalamin associated A Gene

Mmaa - metabolism of cobalamin associated A Gene

  • Gene
  • Protein
  • Agent
  • Ortholog
Rattus norvegicus
Gene ID: 291939 | Gene type: protein coding

About Mmaa

Summary

Predicted to enable GTP binding activity; GTPase activity; and protein homodimerization activity. Predicted to be located in mitochondrion. Human ortholog(s) of this gene implicated in methylmalonic acidemia cblA type. Orthologous to human MMAA (metabolism of cobalamin associated A). [provided by Alliance of Genome Resources, Apr 2022]

Mmaa Products(1)

mRNA Protein Name
NM_001389261.1 NP_001376190.1 methylmalonic aciduria type A protein, mitochondrial
Protein Preferred Names Protein Names

methylmalonic aciduria type A protein, mitochondrial

methylmalonic aciduria (cobalamin deficiency) cblA type

Related Agents

Pre-clinical Phase
Bioactive Molecules (1)
Cat. No. Product Name Effect
Purity Rare Diseases
HY-RS08507 MMAA Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Homo sapiens Mmaa NCBI NCBI:166785