MMADHC

Description		metabolism of cobalamin associated D
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GO Annotations	Cellular Component	Cytoplasm Mitochondrion Cytosol
	Molecular Function	Protein Binding
	Biological Process	Coenzyme Biosynthetic Process Cobalamin Metabolic Process Cofactor Metabolic Process
Pathways		Cobalamin (Cbl, vitamin B12) transport and metabolism Defective MMADHC causes methylmalonic aciduria and homocystinuria type cblD
Drugs
Diseases		Methylmalonic aciduria (MMA)
GWAS		Daytime sleep phenotypes ( 27126917) Liver enzyme levels (alanine transaminase) ( 24124411)
Interacting Genes		2 interacting genes: MMACHC PRNP
Entrez ID		27249
HPRD ID		10781
Ensembl ID		ENSG00000168288
Uniprot IDs		Q9H3L0
PDB IDs		5CUZ 5CV0
Enriched GO Terms of Interacting Partners?
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