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Complement receptor 1

CR1
Protein CR1 PDB 1gkg.png
Available structures
PDB Human UniProt search: PDBe RCSB
Identifiers
Aliases CR1, C3BR, C4BR, CD35, KN, complement component 3b/4b receptor 1 (Knops blood group)
External IDs OMIM: 120620 HomoloGene: 55474 GeneCards: CR1
Genetically Related Diseases
Alzheimer's disease
RNA expression pattern
PBB GE CR1 208488 s at fs.png

PBB GE CR1 217552 x at fs.png

PBB GE CR1 206244 at fs.png
More reference expression data
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_000573
NM_000651

n/a

RefSeq (protein)

NP_000564
NP_000642

n/a

Location (UCSC) Chr 1: 207.5 – 207.64 Mb n/a
PubMed search n/a

1GKG, 1GKN, 1PPQ, 2Q7Z, 2MCY, 2MCZ, 5FO9

NM_000573
NM_000651

n/a

NP_000564
NP_000642

n/a

Complement receptor type 1 (CR1) also known as C3b/C4b receptor or CD35 (cluster of differentiation 35) is a protein that in humans is encoded by the CR1 gene.

This gene is a member of the regulators of complement activation (RCA) family and is located in the 'cluster RCA' region of chromosome 1. The gene encodes a monomeric single-pass type I membrane glycoprotein found on erythrocytes, leukocytes, glomerular podocytes, hyalocytes, and splenic follicular dendritic cells. The Knops blood group system is a system of antigens located on this protein. The protein mediates cellular binding to particles and immune complexes that have activated complement. Decreases in expression of this protein and/or mutations in its gene have been associated with gallbladder carcinomas, mesangiocapillary glomerulonephritis, systemic lupus erythematosus and sarcoidosis. Mutations in this gene have also been associated with a reduction in Plasmodium falciparum rosetting, conferring protection against severe malaria. Alternate allele-specific splice variants, encoding different isoforms, have been characterized. Additional allele specific isoforms, including a secreted form, have been described but have not been fully characterized.


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Wikipedia

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