MMAA

MMAA
Available structures
PDB	Ortholog search: PDBe RCSB
List of PDB id codes
	2WWW
Identifiers
Aliases	MMAA, cblA, methylmalonic aciduria (cobalamin deficiency) cblA type, metabolism of cobalamin associated A
External IDs	OMIM: 607481; MGI: 1923805; HomoloGene: 14586; GeneCards: MMAA; OMA:MMAA - orthologs
Gene location (Human)
Chr.	Chromosome 4 (human)
End	145,660,033 bp
Gene location (Mouse)
Chr.	Chromosome 8 (mouse)
End	80,021,566 bp
RNA expression pattern
	Top expressed in
	secondary oocyte; ; tibialis anterior muscle; ; pancreatic ductal cell; ; testicle; ; deltoid muscle; ; gonad; ; right lobe of liver; ; islet of Langerhans; ; endothelial cell; ; buccal mucosa cell;
	Top expressed in
	interventricular septum; ; saccule; ; otic vesicle; ; right kidney; ; ascending aorta; ; proximal tubule; ; aortic valve; ; motor neuron; ; Paneth cell; ; brown adipose tissue;
	More reference expression data
	n/a
Gene ontology
Molecular function	nucleotide binding; hydrolase activity; GTPase activity; protein binding; GTP binding; identical protein binding; protein homodimerization activity;
Cellular component	mitochondrial matrix; mitochondrion; intracellular anatomical structure;
Biological process	cobalamin metabolic process; cobalamin biosynthetic process; short-chain fatty acid catabolic process; phosphorelay signal transduction system; signal transduction;
	Sources:Amigo / QuickGO
Orthologs
	166785
	109136
	ENSG00000151611
	ENSMUSG00000037022
	Q8IVH4; Q495G5
	Q8C7H1
	NM_172250; NM_001375644
	NM_133823; NM_001363470; NM_001363471; NM_001363472
	NP_758454
	NP_598584; NP_001350399; NP_001350400; NP_001350401
	Wikidata
View/Edit Human	View/Edit Mouse

Methylmalonic aciduria type A protein, mitochondrial also known as MMAA is a protein that in humans is encoded by the MMAA gene.