| BCS1L | 
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| Identifiers | 
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| Aliases | BCS1L, BCS, BCS1, BJS, FLNMS, GRACILE, Hs.6719, MC3DN1, PTD, h-BCS, h-BCS1, BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone | 
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| External IDs | OMIM: 603647; MGI: 1914071; HomoloGene: 3193; GeneCards: BCS1L; OMA:BCS1L - orthologs | 
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| | Gene location (Mouse) | 
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 |  |  | Chr. | Chromosome 1 (mouse) | 
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 |  |  | Band | 1|1 C4 | Start | 74,627,448 bp | 
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 | End | 74,631,602 bp | 
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| | RNA expression pattern | 
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 | Bgee | | Human | Mouse (ortholog) | 
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 | | Top expressed in |  | body of pancreas
 apex of heart
 right uterine tube
 right lobe of liver
 mucosa of transverse colon
 right adrenal gland
 right adrenal cortex
 right lobe of thyroid gland
 body of stomach
 right ovary
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 | | Top expressed in |  | interventricular septum
 soleus muscle
 digastric muscle
 sternocleidomastoid muscle
 medial ganglionic eminence
 myocardium of ventricle
 right kidney
 extraocular muscle
 proximal tubule
 granulocyte
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 |  | More reference expression data | 
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 | BioGPS |  | 
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| Wikidata | 
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Mitochondrial chaperone BCS1 (BCS1L), also known as BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone (h-BCS1), is a protein that in humans is encoded by the BCS1L gene. BCS1L is a chaperone protein involved in the assembly of Ubiquinol Cytochrome c Reductase (complex III), which is located in the inner mitochondrial membrane and is part of the electron transport chain. Mutations in this gene are associated with mitochondrial complex III deficiency (nuclear, 1), GRACILE syndrome, and Bjoernstad syndrome.