MMADHC and EPC2

		MMADHC	EPC2
Description		metabolism of cobalamin associated D	enhancer of polycomb homolog 2
Image			No pdb structure
GO Annotations	Cellular Component	Cytoplasm Mitochondrion Cytosol	Piccolo NuA4 Histone Acetyltransferase Complex
	Molecular Function	Protein Binding	Histone Acetyltransferase Activity
	Biological Process	Cobalamin Metabolic Process	DNA Repair Regulation Of Transcription By RNA Polymerase II Histone Acetylation
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)	Alzheimer's disease biomarkers ( 21123754) Chronotype ( 30696823) Metabolite levels ( 23823483) Protein quantitative trait loci ( 18464913) Pulse pressure ( 30578418) Relative amplitude of rest-activity cycles ( 30120083) Schizophrenia ( 29483656 30285260) Type 2 diabetes ( 32499647 30718926)
Interacting Genes		6 interacting genes: CINP CREB5 MMACHC POU4F2 PRNP TBC1D7	2 interacting genes: EED EZH2
Entrez ID		27249	26122
HPRD ID		10781	13274
Ensembl ID		ENSG00000168288	ENSG00000135999
Uniprot IDs		Q9H3L0	Q52LR7
PDB IDs		5CUZ 5CV0 6X8Z
Enriched GO Terms of Interacting Partners?
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