BCS1L and SLC29A1

Data Source:
BioGRID (affinity chromatography technology)

		BCS1L	SLC29A1
Description		BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone	solute carrier family 29 member 1 (Augustine blood group)
Image		No pdb structure
GO Annotations	Cellular Component	Mitochondrion Mitochondrial Inner Membrane Mitochondrial Respiratory Chain Complex III Integral Component Of Membrane	Plasma Membrane Integral Component Of Plasma Membrane Membrane Integral Component Of Membrane Basolateral Plasma Membrane Apical Plasma Membrane Presynapse Postsynapse
	Molecular Function	Protein Binding ATP Binding ATPase Activity	Neurotransmitter Transmembrane Transporter Activity Nucleoside Transmembrane Transporter Activity Purine Nucleoside Transmembrane Transporter Activity Uridine Transmembrane Transporter Activity
	Biological Process	Mitochondrion Organization Protein Insertion Into Mitochondrial Inner Membrane From Matrix Mitochondrial Respiratory Chain Complex I Assembly Mitochondrial Cytochrome C Oxidase Assembly Mitochondrial Respiratory Chain Complex III Assembly	Neurotransmitter Uptake Nucleobase-containing Compound Metabolic Process Neurotransmitter Transport Lactation Nucleoside Transport Purine Nucleoside Transmembrane Transport Uridine Transport Sleep Adenosine Transport Excitatory Postsynaptic Potential Cellular Response To Glucose Stimulus Cellular Response To Hypoxia Pyrimidine-containing Compound Transmembrane Transport Neurotransmitter Reuptake Transport Across Blood-brain Barrier Nucleoside Transmembrane Transport
Pathways		Mitochondrial protein import	Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane
Drugs			Troglitazone Ethanol Fostamatinib
Diseases		Bjornstad syndrome 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		Male-pattern baldness ( 28196072)	Heel bone mineral density ( 30598549) Mean corpuscular hemoglobin ( 32888494) Mean corpuscular volume ( 27863252) Mean reticulocyte volume ( 32888494) Mean spheric corpuscular volume ( 32888494) Red cell distribution width ( 32888494) Waist-to-hip ratio adjusted for BMI ( 26426971) Waist-to-hip ratio adjusted for BMI (age <50) ( 26426971) Waist-to-hip ratio adjusted for BMI (age >50) ( 26426971) Waist-to-hip ratio adjusted for BMI x sex x age interaction (4df test) ( 26426971)
Interacting Genes		3 interacting genes: DDX24 DNAJA1 MTDH	3 interacting genes: CREB3 HTR2C STK19
Entrez ID		617	2030
HPRD ID		04708	03724
Ensembl ID		ENSG00000074582	ENSG00000112759
Uniprot IDs		A0A024R445 A8JZZ8 Q9Y276	Q99808
PDB IDs			6OB6 6OB7
Enriched GO Terms of Interacting Partners?
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