ATPAF2 and CFAP206

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

Data Source:
BioGRID (two hybrid)

		ATPAF2	CFAP206
Description		ATP synthase mitochondrial F1 complex assembly factor 2	cilia and flagella associated protein 206
Image		No pdb structure	No pdb structure
GO Annotations	Cellular Component	Mitochondrion Cytosol Nuclear Speck	Radial Spoke Motile Cilium A Axonemal Microtubule
	Molecular Function	Protein Binding	Protein Binding
	Biological Process	Proton-transporting ATP Synthase Complex Assembly	Cilium Movement Axoneme 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		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	27 interacting genes: ADAMTSL4 APIP ATPAF2 BANP C1orf94 CEP57L1 GFAP GLYR1 GPRASP2 GSE1 KLHL3 KRT31 KRT40 KRTAP13-1 LZTS2 MDFI RNF138 ROCK1 SAMD3 SOX30 TCF12 TFIP11 TLE5 TMCC2 UBXN11 USHBP1 ZBTB32
Entrez ID		91647	154313
HPRD ID		10599	12863
Ensembl ID		ENSG00000171953	ENSG00000272514
Uniprot IDs		Q8N5M1	Q8IYR0 Q8N771
PDB IDs
Enriched GO Terms of Interacting Partners?
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