FCMR
Immunoglobulin mu Fc receptor
Also known as: FAIM3, FCMR_HUMAN, FcmuR, TOSO
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O60667
- Gene
- FCMR
- Ensembl
- ENSG00000162894
- Chromosome
- 1
- Canonical length
- 390 aa
- Protein class
- Predicted intracellular proteins, Predicted membrane proteins, Predicted secreted proteins
- Subcellular location
- Nucleoplasm,Golgi apparatus,Plasma membrane,Centrosome
- Secretome location
- Secreted to blood
OverviewNCBI Gene
Fc receptors specifically bind to the Fc region of immunoglobulins (Igs) to mediate the unique functions of each Ig class. FAIM3 encodes an Fc receptor for IgM (see MIM 147020) (Kubagawa et al., 2009 [PubMed 19858324]; Shima et al., 2010 [PubMed 20042454]).[supplied by OMIM, Jul 2010]
Canonical amino-acid sequenceUniProt
390 residues, UniProt reviewed canonical sequence.
>O60667|FCMR
1 MDFWLWPLYF LPVSGALRIL PEVKVEGELG GSVTIKCPLP EMHVRIYLCR EMAGSGTCGT
61 VVSTTNFIKA EYKGRVTLKQ YPRKNLFLVE VTQLTESDSG VYACGAGMNT DRGKTQKVTL
121 NVHSEYEPSW EEQPMPETPK WFHLPYLFQM PAYASSSKFV TRVTTPAQRG KVPPVHHSSP
181 TTQITHRPRV SRASSVAGDK PRTFLPSTTA SKISALEGLL KPQTPSYNHH TRLHRQRALD
241 YGSQSGREGQ GFHILIPTIL GLFLLALLGL VVKRAVERRK ALSRRARRLA VRMRALESSQ
301 RPRGSPRPRS QNNIYSACPR RARGADAAGT GEAPVPGPGA PLPPAPLQVS ESPWLHAPSL
361 KTSCEYVSLY HQPAAMMEDS DSDDYINVPALocalizationUniProt · AlphaFold · HPA
Whether an antibody against FCMR 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)
- 0.58
- Highest tissue expression
- 169 nTPM
Expression across tissuesHPA
Tissue
- tonsil: 169 nTPM
- lymph node: 142 nTPM
- spleen: 108 nTPM
- thymus: 72 nTPM
- appendix: 71 nTPM
- small intestine: 56 nTPM
Single-cell type
- b-cells: 297 nCPM
- nk-cells: 108 nCPM
- t-cells: 100 nCPM
- epicardial cells: 91 nCPM
- thymocytes: 62 nCPM
- innate lymphoid cells: 42 nCPM
Immune cell
- naive B-cell: 1,062 nTPM
- memory B-cell: 886 nTPM
- T-reg: 690 nTPM
- naive CD4 T-cell: 485 nTPM
- total PBMC: 417 nTPM
- naive CD8 T-cell: 337 nTPM
Brain region
- white matter: 2.5 nTPM
- thalamus: 2.3 nTPM
- choroid plexus: 2.2 nTPM
- medulla oblongata: 2.2 nTPM
- hypothalamus: 2.1 nTPM
- basal ganglia: 2 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)
- 1.03
- gnomAD pLI
- 0
- DepMap mean gene effect
- -0.08
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cellular defense response
- Fc receptor-mediated immune complex endocytosis
- humoral immune response mediated by circulating immunoglobulin
- negative regulation of apoptotic process
- regulation of B cell receptor signaling pathway
- signal transduction
- immunoglobulin transcytosis in epithelial cells
Molecular functions
- IgM binding
- polymeric immunoglobulin binding
- transmembrane signaling receptor activity
- high-affinity IgM receptor activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads FCMR as an antibody target. Whether an autoantibody or antibody against FCMR could matter depends on whether native FCMR is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
FCMR is annotated at the cell surface, where native FCMR 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 FCMR as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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