FCRL2
Fc receptor-like protein 2
Also known as: CD307b, FCRH2, FCRL2_HUMAN, IRTA4, SPAP1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q96LA5
- Gene
- FCRL2
- Ensembl
- ENSG00000132704
- Chromosome
- 1
- Canonical length
- 508 aa
- Protein class
- CD markers, Predicted membrane proteins
OverviewNCBI Gene
This gene encodes a member of the immunoglobulin receptor superfamily and is one of several Fc receptor-like glycoproteins clustered on the long arm of chromosome 1. The encoded protein has four extracellular C2-type immunoglobulin domains, a transmembrane domain and a cytoplasmic domain that contains one immunoreceptor-tyrosine activation motif and two immunoreceptor-tyrosine inhibitory motifs. This protein may be a prognostic marker for chronic lymphocytic leukemia. Alternatively spliced transcript variants have been described, but their biological validity has not been determined. [provided by RefSeq, Apr 2009]
Canonical amino-acid sequenceUniProt
508 residues, UniProt reviewed canonical sequence.
>Q96LA5|FCRL2
1 MLLWSLLVIF DAVTEQADSL TLVAPSSVFE GDSIVLKCQG EQNWKIQKMA YHKDNKELSV
61 FKKFSDFLIQ SAVLSDSGNY FCSTKGQLFL WDKTSNIVKI KVQELFQRPV LTASSFQPIE
121 GGPVSLKCET RLSPQRLDVQ LQFCFFRENQ VLGSGWSSSP ELQISAVWSE DTGSYWCKAE
181 TVTHRIRKQS LQSQIHVQRI PISNVSLEIR APGGQVTEGQ KLILLCSVAG GTGNVTFSWY
241 REATGTSMGK KTQRSLSAEL EIPAVKESDA GKYYCRADNG HVPIQSKVVN IPVRIPVSRP
301 VLTLRSPGAQ AAVGDLLELH CEALRGSPPI LYQFYHEDVT LGNSSAPSGG GASFNLSLTA
361 EHSGNYSCEA NNGLGAQCSE AVPVSISGPD GYRRDLMTAG VLWGLFGVLG FTGVALLLYA
421 LFHKISGESS ATNEPRGASR PNPQEFTYSS PTPDMEELQP VYVNVGSVDV DVVYSQVWSM
481 QQPESSANIR TLLENKDSQV IYSSVKKSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against FCRL2 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
- Cell surface
- Secreted
- No
- Transmembrane segments
- 1
- Mean surface accessibility (rSASA)
- 0.4
- Highest tissue expression
- 33 nTPM
Expression across tissuesHPA
Tissue
- spleen: 33 nTPM
- tonsil: 24 nTPM
- lymph node: 23 nTPM
- small intestine: 20 nTPM
- appendix: 12 nTPM
- bone marrow: 2.5 nTPM
Single-cell type
- b-cells: 141 nCPM
- plasma cells: 55 nCPM
- neutrophils: 6.9 nCPM
- thymocytes: 5.9 nCPM
- conjunctival goblet cells: 4.9 nCPM
- gastric chief cells: 4.4 nCPM
Immune cell
- memory B-cell: 30 nTPM
- naive B-cell: 19 nTPM
- basophil: 0.7 nTPM
- total PBMC: 0.6 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
Brain region
- white matter: 3.6 nTPM
- cerebral cortex: 3 nTPM
- medulla oblongata: 3 nTPM
- pons: 2.6 nTPM
- hypothalamus: 2.5 nTPM
- spinal cord: 2.5 nTPM
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)
- 1.12
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.48
- DepMap mean gene effect
- 0
- 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
InteractionsUniProt · HPA
Protein binding partners of FCRL2 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads FCRL2 as an antibody target. Whether an autoantibody or antibody against FCRL2 could matter depends on whether native FCRL2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
FCRL2 is annotated at the cell surface, where native FCRL2 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label FCRL2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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