MMAB

MMAB
Available structures
PDB	Ortholog search: PDBe RCSB
List of PDB id codes
	2IDX
Identifiers
Aliases	MMAB, ATR, CFAP23, cblB, cob, methylmalonic aciduria (cobalamin deficiency) cblB type, metabolism of cobalamin associated B
External IDs	OMIM: 607568; MGI: 1924947; HomoloGene: 12680; GeneCards: MMAB; OMA:MMAB - orthologs
Gene location (Human)
Chr.	Chromosome 12 (human)
End	109,573,580 bp
Gene location (Mouse)
Chr.	Chromosome 5 (mouse)
End	114,582,121 bp
RNA expression pattern
	Top expressed in
	right lobe of liver; ; right adrenal cortex; ; left adrenal gland; ; left adrenal cortex; ; apex of heart; ; C1 segment; ; pancreatic ductal cell; ; mucosa of transverse colon; ; right auricle of heart; ; olfactory zone of nasal mucosa;
	Top expressed in
	lumbar spinal ganglion; ; muscle of thigh; ; interventricular septum; ; otic vesicle; ; neural layer of retina; ; saccule; ; right kidney; ; ascending aorta; ; myocardium of ventricle; ; neural tube;
	More reference expression data
	More reference expression data
Gene ontology
Molecular function	transferase activity; nucleotide binding; cob(I)yrinic acid a,c-diamide adenosyltransferase activity; ATP binding; protein binding; cobalamin binding;
Cellular component	mitochondrial matrix; mitochondrion;
Biological process	cobalamin metabolic process; cobalamin biosynthetic process;
	Sources:Amigo / QuickGO
Orthologs
	326625
	77697
	ENSG00000139428
	ENSMUSG00000029575
	Q96EY8
	Q9D273
	NM_052845
	NM_029956; NM_001347398
	NP_443077
	NP_001334327; NP_084232
	Wikidata
View/Edit Human	View/Edit Mouse

Cob(I)yrinic acid a,c-diamide adenosyltransferase, mitochondrial is an enzyme that in humans is encoded by the MMAB gene.