Homo sapiens Gene: CFHR4 | |||||||||||||||||||
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Summary | |||||||||||||||||||
InnateDB Gene | IDBG-105525.6 | ||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||
Gene Symbol | CFHR4 | ||||||||||||||||||
Gene Name | complement factor H-related 4 | ||||||||||||||||||
Synonyms | CFHL4; FHR-4; FHR4 | ||||||||||||||||||
Species | Homo sapiens | ||||||||||||||||||
Ensembl Gene | ENSG00000134365 | ||||||||||||||||||
Encoded Proteins |
complement factor H-related 4
complement factor H-related 4
complement factor H-related 4
complement factor H-related 4
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Protein Structure | |||||||||||||||||||
Useful resources | Stemformatics EHFPI ImmGen | ||||||||||||||||||
Entrez Gene | |||||||||||||||||||
Summary |
This gene is a member of the complement factor H (CFH) gene family, and encodes one of the 5 CFH-related (CFHR) proteins. These 5 genes are closely linked to the CFH gene on chromosome 1q31-q32. The CFHRs are secreted plasma proteins synthesized primarily by the hepatocytes, and composed of highly-related short consensus repeats (SCRs). This protein enhances the cofactor activity of CFH, and is involved in complement regulation. It can associate with lipoproteins and may play a role in lipid metabolism. Alternatively spliced transcript variants encoding different isoforms (varying in the number of SCRs) have been described for this gene. [provided by RefSeq, Jan 2011] |
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Gene Information | |||||||||||||||||||
Type | Protein coding | ||||||||||||||||||
Genomic Location | Chromosome 1:196850241-196918972 | ||||||||||||||||||
Strand | Forward strand | ||||||||||||||||||
Band | q31.3 | ||||||||||||||||||
Transcripts |
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Interactions | |||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 4 experimentally validated interaction(s) in this database.
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Gene Ontology | |||||||||||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Orthologs | |||||||||||||||||||
No orthologs found for this gene | |||||||||||||||||||
Cross-References | |||||||||||||||||||
SwissProt | Q92496 | ||||||||||||||||||
TrEMBL | V9GYX2 | ||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||
Entrez Gene | 10877 | ||||||||||||||||||
UniGene | Hs.710100 | ||||||||||||||||||
RefSeq | NM_001201550 NM_001201551 NM_006684 XM_006711128 XM_006711129 XM_006711130 XM_006711132 XM_006711134 | ||||||||||||||||||
HUGO | HGNC:16979 | ||||||||||||||||||
OMIM | 605337 | ||||||||||||||||||
CCDS | CCDS41451 CCDS55671 | ||||||||||||||||||
HPRD | |||||||||||||||||||
IMGT | |||||||||||||||||||
EMBL | AF190816 AJ640130 AK292752 AL139418 BC074957 BX248415 CH471067 X98337 | ||||||||||||||||||
GenPept | AAF05951 AAH74957 BAF85441 CAA66980 CAG26679 CAH70075 CAI21980 EAW91266 | ||||||||||||||||||
RNA Seq Atlas | 10877 | ||||||||||||||||||