MRPS12 and BCS1L

		MRPS12	BCS1L
Description		mitochondrial ribosomal protein S12	BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone
Image			No pdb structure
GO Annotations	Cellular Component	Mitochondrial Inner Membrane Mitochondrial Ribosome Mitochondrial Small Ribosomal Subunit Ribosome	Mitochondrion Mitochondrial Respiratory Chain Complex III Integral Component Of Membrane
	Molecular Function	RNA Binding Structural Constituent Of Ribosome Protein Binding	Protein Binding ATP Binding
	Biological Process	Translation Mitochondrial Translation Mitochondrial Translational Elongation Mitochondrial Translational Termination	Mitochondrion Organization Mitochondrial Respiratory Chain Complex I Assembly Mitochondrial Respiratory Chain Complex IV Assembly Mitochondrial Respiratory Chain Complex III Assembly
Pathways		Mitochondrial translation initiation Mitochondrial translation elongation Mitochondrial translation elongation Mitochondrial translation termination	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)
Interacting Genes		6 interacting genes: BCS1L CRMP1 ERG28 LRIF1 SPINK7 UNC119	14 interacting genes: AOX1 ARHGAP18 CD28 CLK1 CTLA4 DDX24 DNAJA1 MRPS12 MTDH ORC2 RP9 RPE SLC29A1 WDFY1
Entrez ID		6183	617
HPRD ID		04316	04708
Ensembl ID		ENSG00000128626	ENSG00000074582
Uniprot IDs		A0A024R0H2 O15235	A0A024R445 A8JZZ8 Q9Y276
PDB IDs		3J9M 6NU2 6NU3
Enriched GO Terms of Interacting Partners?
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