XB-FEAT-995375: Difference between revisions
Jump to navigation
Jump to search
imported>Xenbase gene generator No edit summary |
imported>Xenbase |
||
| Line 1: | Line 1: | ||
=c1r= | =c1r= | ||
This is the community wiki page for the gene ''c1r'' please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase | This is the community wiki page for the gene ''c1r'' please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase | ||
=nomenclature changes= | |||
02.25.20 | |||
name changed from 'complement component 1, r subcomponent' to 'complement C1r', following Human nomenclature. | |||
=Summary fro human CR1 from NCBI= | |||
This gene encodes a member of the peptidase S1 protein family. The encoded protein is a proteolytic subunit in the complement system C1 complex. The complement system acts as a mediator in the innate immune response by ultimately triggering phagocytosis, inflammation, and rupturing the bacterial cell wall. Mutations in this gene are associated with Ehlers-Danlos Syndrome. [provided by RefSeq, Dec 2018] | |||
Latest revision as of 06:29, 26 February 2020
c1r
This is the community wiki page for the gene c1r please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase
nomenclature changes
02.25.20 name changed from 'complement component 1, r subcomponent' to 'complement C1r', following Human nomenclature.
Summary fro human CR1 from NCBI
This gene encodes a member of the peptidase S1 protein family. The encoded protein is a proteolytic subunit in the complement system C1 complex. The complement system acts as a mediator in the innate immune response by ultimately triggering phagocytosis, inflammation, and rupturing the bacterial cell wall. Mutations in this gene are associated with Ehlers-Danlos Syndrome. [provided by RefSeq, Dec 2018]