Mmaa - methylmalonic aciduria (cobalamin deficiency) type A Gene

Mus musculus

Also known as 2810018E08Rik

Gene ID: 109136 | Gene type: protein coding

About Mmaa

Summary

Predicted to enable several functions, including GTP binding activity; GTPase activity; and protein homodimerization activity. Predicted to be involved in cobalamin metabolic process. Predicted to be located in mitochondrion. Is expressed in several structures, including alimentary system; cardiovascular system; genitourinary system; lung; and trophectoderm. 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(4)

mRNA	Protein	Name
NM_001363470.1	NP_001350399.1	methylmalonic aciduria type A homolog, mitochondrial isoform a precursor
NM_001363471.1	NP_001350400.1	methylmalonic aciduria type A homolog, mitochondrial isoform b
NM_001363472.1	NP_001350401.1	methylmalonic aciduria type A homolog, mitochondrial isoform b
NM_133823.5	NP_598584.2	methylmalonic aciduria type A homolog, mitochondrial isoform a precursor

Protein Preferred Names

Protein Names

methylmalonic aciduria type A homolog, mitochondrial

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

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