ATPAF2 and MAGEA6

Number of citations of the paper that reports this interaction (PubMedID 25910212)
127

Data Source:
BioGRID (two hybrid)

		ATPAF2	MAGEA6
Description		ATP synthase mitochondrial F1 complex assembly factor 2	MAGE family member A6
Image		No pdb structure	No pdb structure
GO Annotations	Cellular Component	Mitochondrion Cytosol Nuclear Speck	Cellular_component
	Molecular Function	Protein Binding	Molecular_function Protein Binding
	Biological Process	Proton-transporting ATP Synthase Complex Assembly	Biological_process
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		anorexia nervosa, attention-deficit/hyperactivity disorder, autism spectrum disorder, bipolar disorder, major depression, obsessive-compulsive disorder, schizophrenia, or Tourette syndrome (pleiotropy) ( 31835028) Schizophrenia ( 28991256 25056061 29483656)
Interacting Genes		24 interacting genes: APP ATP5F1A ATP5F1B BEGAIN CFAP206 DDIT3 EBF1 EWSR1 IKZF3 KRT40 LNX1 LRRFIP2 LZTS2 MAGEA6 PAK5 PKP4 PRDM14 RAD54B REL RPIA SORBS2 TP53BP2 TRIM23 TRIM27	40 interacting genes: ACOT7 AKAP9 ANKRD26P1 ATP6V1G1 ATPAF2 BCL7B BET1 CCDC146 CTF1 ELMOD3 EXOC5 FAM214A FRMPD1 GFOD1 HAUS1 HLA-DRB4 IQUB KLHL38 LCORL LIN37 LSM2 MCM7 MED21 MIPOL1 MORN3 NCK2 PDE4D RASSF4 RCOR3 RPL37A S100A14 SH2D4A SNAP47 SNX4 STAMBPL1 STX5 TRIM26 TRIM28 TULP3 TXNDC9
Entrez ID		91647	4105
HPRD ID		10599	02168
Ensembl ID		ENSG00000171953	ENSG00000197172
Uniprot IDs		Q8N5M1	P43360
PDB IDs
Enriched GO Terms of Interacting Partners?
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