| C5 |
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| Available structures |
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| PDB | Ortholog search: PDBe RCSB |
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| List of PDB id codes |
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1CFA, 1KJS, 1XWE, 3CU7, 3HQA, 3HQB, 3KLS, 3KM9, 3PRX, 3PVM, 4A5W, 4E0S, 4P39, 4UU9, 5I5K, 5HCE, 5HCC, 5HCD |
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| Identifiers |
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| Aliases | C5, C5D, C5a, C5b, CPAMD4, ECLZB, complement component 5, complement C5 |
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| External IDs | OMIM: 120900; MGI: 96031; HomoloGene: 20412; GeneCards: C5; OMA:C5 - orthologs |
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| Gene location (Human) |
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| | Chr. | Chromosome 9 (human)[1] |
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| | Band | 9q33.2 | Start | 120,932,642 bp[1] |
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| End | 121,075,195 bp[1] |
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| Gene location (Mouse) |
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| | Chr. | Chromosome 2 (mouse)[2] |
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| | Band | 2 B|2 23.22 cM | Start | 34,873,343 bp[2] |
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| End | 34,951,450 bp[2] |
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| RNA expression pattern |
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| Bgee | | Human | Mouse (ortholog) |
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| Top expressed in | - right lobe of liver
- oocyte
- body of pancreas
- secondary oocyte
- Achilles tendon
- gonad
- tibial nerve
- testicle
- Descending thoracic aorta
- ventricular zone
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| | Top expressed in | - left lobe of liver
- right lung lobe
- left lung
- left lung lobe
- gallbladder
- granulocyte
- fetal liver hematopoietic progenitor cell
- human fetus
- neural groove
- embryo
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| | More reference expression data |
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| BioGPS | |
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| Gene ontology |
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| Molecular function | | | Cellular component | | | Biological process | | | Sources:Amigo / QuickGO |
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| Wikidata |
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Complement component 5 is a protein that in humans is encoded by the C5 gene.[5]
Complement component 5 is involved in the complement system. It is cleaved into C5a and C5b:
Deficiency is thought to cause Leiner's disease.