Mmab - metabolism of cobalamin associated B Gene

Species: Rattus norvegicus

Gene Type: protein coding
Gene ID: 687861

Summary

Predicted to enable cob(I)yrinic acid a,c-diamide adenosyltransferase activity and cobalamin binding activity. Human ortholog(s) of this gene implicated in inherited metabolic disorder and methylmalonic acidemia cblB type. Orthologous to human MMAB (metabolism of cobalamin associated B). [provided by Alliance of Genome Resources, Apr 2022]

Mmab Products (1)

mRNA Protein Name
NM_001398937.1 NP_001385866.1 metabolism of cobalamin associated B
Protein Preferred Names Protein Names

corrinoid adenosyltransferase

metabolism of cobalamin associated B

  • cob(I)yrinic acid a,c-diamide adenosyltransferase, mitochondrial

  • methylmalonic aciduria (cobalamin deficiency) cblB type

  • methylmalonic aciduria (cobalamin deficiency) type B homolog

Related Agents

  • Pre-clinical Phase

Pre-clinical Phase

Bioactive Molecules (3)
Cat. No. Product Name
Effect
Purity
Rare Diseases
HY-RS08508 MMAB Human Pre-designed siRNA Set A Pre-designed Set / Unkown
HY-RS22238 Mmab Mouse Pre-designed siRNA Set A Pre-designed Set / Unkown
HY-RS28760 Mmab Rat Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Homo sapiens Mmab NCBI NCBI:326625