DPCD and NDUFS7

Data Source:
BioGRID (affinity chromatography technology)

		DPCD	NDUFS7
Description		deleted in primary ciliary dyskinesia homolog (mouse)	NADH:ubiquinone oxidoreductase core subunit S7
Image		No pdb structure
GO Annotations	Cellular Component	Extracellular Region Nucleus	Mitochondrial Respiratory Chain Complex I Mitochondrial Matrix
	Molecular Function	Protein Binding	NADH Dehydrogenase Activity Protein Binding NADH Dehydrogenase (ubiquinone) Activity Oxidoreductase Activity, Acting On NAD(P)H, Quinone Or Similar Compound As Acceptor Metal Ion Binding Quinone Binding 4 Iron, 4 Sulfur Cluster Binding
	Biological Process	Epithelial Cilium Movement Involved In Extracellular Fluid Movement Spermatogenesis Determination Of Left/right Symmetry Lateral Ventricle Development Third Ventricle Development Flagellated Sperm Motility Left/right Pattern Formation	Mitochondrial Electron Transport, NADH To Ubiquinone Aerobic Respiration Electron Transport Coupled Proton Transport Mitochondrial Respiratory Chain Complex I Assembly
Pathways			Respiratory electron transport Complex I biogenesis
Drugs			NADH
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		Mean corpuscular volume ( 32888494)
Interacting Genes		2 interacting genes: APP RUVBL2	3 interacting genes: ARRB2 ENO2 MT-ND1
Entrez ID		25911	374291
HPRD ID		13247	03491
Ensembl ID		ENSG00000166171	ENSG00000115286
Uniprot IDs		Q5JQQ4 Q9BVM2	O75251 Q6ZS38 Q7LD69
PDB IDs			5XTB 5XTD 5XTH 5XTI
Enriched GO Terms of Interacting Partners?
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