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

Mus musculus

Also known as ATR; 9130222L19Rik

Gene ID: 77697 | Gene type: protein coding

About Mmab

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

Related Agents

Pre-clinical Phase

Bioactive Molecules (2)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS08508	MMAB Human Pre-designed siRNA Set A	Pre-designed Sets	/	Unkown
HY-RS22238	Mmab Mouse Pre-designed siRNA Set A	Pre-designed Sets	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Homo sapiens	Mmab	NCBI	NCBI:326625

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