Protein-coding gene in the species Homo sapiens
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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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.[5][6][7]