BCS1L

Description		BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone
Image		No pdb structure
GO Annotations	Cellular Component	Mitochondrion Mitochondrial Inner Membrane Mitochondrial Respiratory Chain Complex III Integral Component Of Membrane
	Molecular Function	Protein Binding ATP Binding ATPase 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
Pathways		Mitochondrial protein import
Drugs
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)
Novel Interacting Genes		11 novel interacting genes: AOX1 ARHGAP18 CD28 CLK1 CTLA4 MRPS12 ORC2 RP9 RPE SLC29A1 WDFY1
Interacting Genes		3 interacting genes: DDX24 DNAJA1 MTDH
Entrez ID		617
HPRD ID		04708
Ensembl ID		ENSG00000074582
Uniprot IDs		A0A024R445 A8JZZ8 Q9Y276
PDB IDs
Enriched GO Terms of Interacting Partners?
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