| CFH |
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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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4ONT, 1HAQ, 1HCC, 1HFH, 1HFI, 2BZM, 2G7I, 2IC4, 2JGW, 2JGX, 2KMS, 2QFG, 2QFH, 2RLP, 2RLQ, 2UWN, 2V8E, 2W80, 2W81, 2WII, 2XQW, 3GAU, 3GAV, 3GAW, 3KXV, 3KZJ, 3OXU, 3R62, 3RJ3, 3SW0, 4AYD, 4AYE, 4AYI, 4AYM, 4B2R, 4B2S, 4J38, 4K12, 4ZH1 |
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| Identifiers |
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| Aliases | CFH, AHUS1, AMBP1, ARMD4, ARMS1, CFHL3, FH, FHL1, HF, HF1, HF2, HUS, complement factor H |
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| External IDs | OMIM: 134370; MGI: 88385; HomoloGene: 20086; GeneCards: CFH; OMA:CFH - orthologs |
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| Gene location (Mouse) |
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| | Chr. | Chromosome 1 (mouse) |
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| | Band | 1 61.62 cM|1 F | Start | 140,012,446 bp |
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| End | 140,111,502 bp |
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| Wikidata |
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Factor H (FH) is a soluble glycoprotein and a member of the regulators of complement activation (RCA) family. It functions as a complement control protein and plays a critical role in regulating the complement system, particularly the alternative pathway. Factor H is a large molecule with a molecular weight of approximately 155 kilodaltons and circulates in human blood plasma at concentrations typically ranging from 200–300 micrograms per milliliter.