COA5

Description		cytochrome c oxidase assembly factor 5
Image		No pdb structure
GO Annotations	Cellular Component	Mitochondrion
	Molecular Function	Protein Binding
	Biological Process	Mitochondrial Cytochrome C Oxidase Assembly
Pathways
Drugs
Diseases		Mitochondrial respiratory chain deficiencies (MRCD), including: Mitochondrial complex I deficiency (MT-C1D); Complex II deficiency (MT-C2D); Complex III deficiency (MT-C3D); Complex IV deficiency (MT-C4D); Complex V deficiency (MT-ATPSD); Leigh syndrome (LS); Kearns-Sayre Syndrome (KSS); LCHD deficiency (LCHD); Leber Hereditary Optic Neuropathy (LHON); Myoclonic Epilepsy and Ragged-Red Fiber Disease (MERRF); NARP; MELAS; ACAD9 deficiency; HADH deficiency; HIBCH deficiency; GRACILE syndrome
GWAS
Interacting Genes		5 interacting genes: APP CYSRT1 KRT31 KRTAP1-3 TCF4
Entrez ID		493753
HPRD ID		17563
Ensembl ID		ENSG00000183513
Uniprot IDs		Q86WW8
PDB IDs
Enriched GO Terms of Interacting Partners?
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