CFHR2
Complement factor H-related protein 2
Also known as: CFHL2, FHR2, FHR2_HUMAN, HFL3
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P36980
- Gene
- CFHR2
- Ensembl
- ENSG00000080910
- Chromosome
- 1
- Canonical length
- 270 aa
- Protein class
- Plasma proteins, Predicted intracellular proteins, Predicted secreted proteins
- Secretome location
- Secreted to blood
- Quaternary structure
- Homodimer
OverviewNCBI Gene
This gene belongs to a family of complement factor H-related genes (CFHR), which are clustered together with complement factor H gene on chromosome 1, and are involved in regulation of complement. Mutations in CFHR genes have been associated with dense deposit disease and atypical haemolytic-uraemic syndrome. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Aug 2015]
Canonical amino-acid sequenceUniProt
270 residues, UniProt reviewed canonical sequence.
>P36980|CFHR2
1 MWLLVSVILI SRISSVGGEA MFCDFPKINH GILYDEEKYK PFSQVPTGEV FYYSCEYNFV
61 SPSKSFWTRI TCAEEGWSPT PKCLRLCFFP FVENGHSESS GQTHLEGDTV QIICNTGYRL
121 QNNENNISCV ERGWSTPPKC RSTISAEKCG PPPPIDNGDI TSFLLSVYAP GSSVEYQCQN
181 LYQLEGNNQI TCRNGQWSEP PKCLDPCVIS QEIMEKYNIK LKWTNQQKLY SRTGDIVEFV
241 CKSGYHPTKS HSFRAMCQNG KLVYPSCEEKLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CFHR2 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Secreted
- Secreted
- Yes
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.36
- Highest tissue expression
- 1,262 nTPM
Expression across tissuesHPA
Tissue
- liver: 1,262 nTPM
- kidney: 0.4 nTPM
- spleen: 0.3 nTPM
- adipose tissue: 0.1 nTPM
- appendix: 0.1 nTPM
- skeletal muscle: 0.1 nTPM
Single-cell type
- hepatocytes: 1,476 nCPM
- kupffer cells: 10 nCPM
- hepatic stellate cells: 6.5 nCPM
- cholangiocytes: 3.9 nCPM
- hofbauer cells: 1.1 nCPM
- monocytes: 1 nCPM
Immune cell
- basophil: 0.2 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- cerebral cortex: 0.7 nTPM
- white matter: 0.7 nTPM
- cerebellum: 0.6 nTPM
- choroid plexus: 0.6 nTPM
- hippocampal formation: 0.6 nTPM
- basal ganglia: 0.5 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about CFHR2.
Disease | ImmuneIEDB
Conditions an epitope on CFHR2 was assayed in.
- rheumatoid arthritis B cell
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 1.82
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.9
- DepMap mean gene effect
- 0.06
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 2% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads CFHR2 as an antibody target. Whether an autoantibody or antibody against CFHR2 could matter depends on whether native CFHR2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CFHR2 is annotated as secreted, so native CFHR2 circulates and is directly accessible to antibodies. Secreted and cell-surface proteins are the autoantibody targets most likely to act like drugs, blocking or depleting the native protein.
Annotation status
The present source text does not explicitly label CFHR2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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