MMADHC

Description		metabolism of cobalamin associated D
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GO Annotations	Cellular Component	Cytoplasm Mitochondrion Cytosol
	Molecular Function	Protein Binding
	Biological Process	Cobalamin 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) Neonatal total 25-hydroxyvitamin D levels (fetal genetic effect) ( 32047095)
Novel Interacting Genes		1 novel interacting genes: EPC2
Interacting Genes		6 interacting genes: CINP CREB5 MMACHC POU4F2 PRNP TBC1D7
Entrez ID		27249
HPRD ID		10781
Ensembl ID		ENSG00000168288
Uniprot IDs		Q9H3L0
PDB IDs		5CUZ 5CV0 6X8Z
Enriched GO Terms of Interacting Partners?
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