Mmab - methylmalonic aciduria (cobalamin deficiency) cblB type homolog (human) Gene

Also Known as ATR; 9130222L19Rik

Species: Mus musculus

Gene Type: protein coding
Gene ID: 77697

Summary

Predicted to enable cob(I)yrinic acid a,c-diamide adenosyltransferase activity and cobalamin binding activity. Predicted to be involved in cobalamin metabolic process. Located in mitochondrion. Is expressed in several structures, including alimentary system; cardiovascular system; lung; nervous system; and trophectoderm. 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 (2)

mRNA Protein Name
NM_001347398.1 NP_001334327.1 corrinoid adenosyltransferase MMAB isoform 2 precursor
NM_029956.4 NP_084232.1 corrinoid adenosyltransferase MMAB isoform 1 precursor
Protein Preferred Names Protein Names

corrinoid adenosyltransferase MMAB

corrinoid adenosyltransferase

  • ATP:co(I)rrinoid adenosyltransferase MMAB

  • ATP:cob(I)alamin adenosyltransferase

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

  • cob(II)alamin adenosyltransferase

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

  • cobinamide/cobalamin

Orthologs Information

Species Symbol Source ID
Homo sapiens Mmab NCBI NCBI:326625