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

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

种属: Mus musculus

同用名: ATR; 9130222L19Rik

基因 ID: 77697 | 基因类型: protein coding

关于 Mmab

功能概要

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 基因产物(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
蛋白主名 其他名称

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

直系同源

种属 基因名 来源 基因 ID
Homo sapiens Mmab NCBI NCBI:326625