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FCGR2B (Fc gamma receptor IIb)

Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
2213
Gene nameGene Name - the full gene name approved by the HGNC.
Fc gamma receptor IIb
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
FCGR2B
SynonymsGene synonyms aliases
CD32, CD32B, FCG2, FCGR2, FCGR2C, FcGRIIB, FcRII-c, FcgammaRIIb, IGFR2
ChromosomeChromosome number
1
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
1q23.3
SummarySummary of gene provided in NCBI Entrez Gene.
The protein encoded by this gene is a low affinity receptor for the Fc region of immunoglobulin gamma complexes. The encoded protein is involved in the phagocytosis of immune complexes and in the regulation of antibody production by B-cells. Variations in
SNPsSNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs1050501 T>A,C Risk-factor, protective Genic downstream transcript variant, downstream transcript variant, coding sequence variant, missense variant
rs3219018 G>C Risk-factor Upstream transcript variant, intron variant, genic upstream transcript variant
miRNAmiRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT438477 hsa-miR-18a-5p qRT-PCR, Western blot 24169826
MIRT438477 hsa-miR-18a-5p qRT-PCR, Western blot 24169826
MIRT993861 hsa-miR-1183 CLIP-seq
MIRT993862 hsa-miR-194 CLIP-seq
MIRT993863 hsa-miR-4423-3p CLIP-seq
Transcription factors
Transcription factor Regulation Reference
GATA4 Unknown 15153544
YY1 Unknown 15153544
Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001540 Function Amyloid-beta binding IPI 23921129
GO:0001540 Function Amyloid-beta binding TAS 26871627
GO:0001811 Process Negative regulation of type I hypersensitivity ISS 26683154
GO:0001814 Process Negative regulation of antibody-dependent cellular cytotoxicity TAS 26683154
GO:0001818 Process Negative regulation of cytokine production TAS 26683154
Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM
HGNC
e!Ensembl
Protein
UniProt ID P31994
Protein name Low affinity immunoglobulin gamma Fc region receptor II-b (IgG Fc receptor II-b) (CDw32) (Fc-gamma RII-b) (Fc-gamma-RIIb) (FcRII-b) (CD antigen CD32)
Protein function Receptor for the Fc region of complexed or aggregated immunoglobulins gamma. Low affinity receptor. Involved in a variety of effector and regulatory functions such as phagocytosis of immune complexes and modulation of antibody production by B-ce
PDB 2FCB , 3WJJ , 5OCC
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF13895 Ig_2
49 128
Immunoglobulin domain
Domain
PF13895 Ig_2
132 214
Immunoglobulin domain
Domain
Sequence
MGILSFLPVLATESDWADCKSPQPWGHMLLWTAVLFLAPVAGTPAAPPKAVLKLEPQWIN
VLQEDSVTLTCRGTHSPESDSIQWFHNGNLIPTHTQPSYRFKANNNDSGEYTCQTGQTSL
SDPVHLTV
LSEWLVLQTPHLEFQEGETIVLRCHSWKDKPLVKVTFFQNGKSKKFSRSDPN
FSIPQANHSHSGDYHCTGNIGYTLYSSKPVTITV
QAPSSSPMGIIVAVVTGIAVAAIVAA
VVALIYCRKKRISALPGYPECREMGETLPEKPANPTNPDEADKVGAENTITYSLLMHPDA
LEEPDDQNRI
Sequence length 310
Interactions View interactions
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
 
KEGG
 
Reactome
  Virion - Ebolavirus, Lyssavirus and Morbillivirus
Phagosome
Osteoclast differentiation
B cell receptor signaling pathway
Fc gamma R-mediated phagocytosis
Staphylococcus aureus infection
Tuberculosis
Measles
  Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell
Associated diseases
Causal
Disease name Disease term dbSNP ID References
Anemia Anemia, Hemolytic rs118204044, rs118204045, rs118204046, rs121918330, rs869320719, rs869312029, rs121918332, rs869320724, rs767094129, rs786205058, rs786205059, rs137853119, rs137853120, rs137853121, rs1384933966, rs137853122, rs137853123, rs786205060, rs267607121, rs121908584, rs80338697, rs80338699, rs120074166, rs120074167, rs1050828, rs74575103, rs137852314, rs5030868, rs137852316, rs137852317, rs137852318, rs137852319, rs137852320, rs137852321, rs137852322, rs137852323, rs137852324, rs72554665, rs387906468, rs5030872, rs137852326, rs137852333, rs137852327, rs137852328, rs137852329, rs137852330, rs137852331, rs137852332, rs137852334, rs137852335, rs137852336, rs137852339, rs76645461, rs137852340, rs137852341, rs78478128, rs137852343, rs137852344, rs137852345, rs587776730, rs137852346, rs137852347, rs137852349, rs2070404412, rs2070350038, rs2070350009, rs137852303, rs137852304, rs33946267, rs34378160, rs33933298, rs11549407, rs35724775, rs34598529, rs41469945, rs267607201, rs80338694, rs80338696, rs387907018, rs398123546, rs78365220, rs587777100, rs587777101, rs483352840, rs869312752, rs765487627, rs1557229599, rs1557230040, rs1555524842, rs782090947, rs1358275550, rs1557229736, rs1557230573, rs1556323334, rs1233124208, rs1293528130, rs146864395, rs1595503440, rs1603411214, rs137852325, rs1575247302, rs1603411177, rs1336651679, rs782322505
Arthritis Arthritis rs1594890601, rs1594882933, rs184370809, rs776489319, rs1594883470
Autoimmune diseases Autoimmune Diseases rs41285370, rs869025224 10848805
Neutropenia Neutropenia rs879253882 10848805
Unknown
Disease name Disease term dbSNP ID References
Leukopenia Leukopenia
Lupus erythematosus Lupus Erythematosus, Systemic 12115230, 20385827, 23943494
Nephritis Nephritis
Nonbacterial verrucal endocardiosis Libman-Sacks Disease

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