Gene Gene information from NCBI Gene database.
Entrez ID 2215
Gene name Fc gamma receptor IIIb
Gene symbol FCGR3B
Synonyms (NCBI Gene)
CD16CD16-ICD16ACD16bFCG3FCGR3FCGR3AFCR-10FCRIIIFCRIIIb
Chromosome 1
Chromosome location 1q23.3
Summary The protein encoded by this gene is a low affinity receptor for the Fc region of gamma immunoglobulins (IgG). The encoded protein acts as a monomer and can bind either monomeric or aggregated IgG. This gene may function to capture immune complexes in the
SNPs SNP information provided by dbSNP.
4
SNP ID Visualize variation Clinical significance Consequence
rs448740 T>A,C Benign, pathogenic Coding sequence variant, missense variant
rs2290834 T>C Benign, pathogenic Coding sequence variant, missense variant
rs147574249 T>A,C Pathogenic Missense variant, coding sequence variant
rs200688856 G>A,C,T Pathogenic Missense variant, coding sequence variant, synonymous variant
miRNA miRNA information provided by mirtarbase database.
28
miRTarBase ID miRNA Experiments Reference
MIRT528784 hsa-miR-6729-3p PAR-CLIP 22012620
MIRT528782 hsa-miR-1224-3p PAR-CLIP 22012620
MIRT528781 hsa-miR-4286 PAR-CLIP 22012620
MIRT528780 hsa-miR-136-5p PAR-CLIP 22012620
MIRT528779 hsa-miR-942-5p PAR-CLIP 22012620
Transcription factors Transcription factors information provided by TRRUST V2 database.
2
Transcription factor Regulation Reference
GATA4 Unknown 15153544
YY1 Unknown 15153544
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
17
GO ID Ontology Definition Evidence Reference
GO:0001788 Process Antibody-dependent cellular cytotoxicity IBA
GO:0005576 Component Extracellular region IEA
GO:0005576 Component Extracellular region TAS
GO:0005886 Component Plasma membrane IDA 1825220
GO:0005886 Component Plasma membrane IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
610665 3620 ENSG00000162747
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
O75015
Protein name Low affinity immunoglobulin gamma Fc region receptor III-B (Fc-gamma RIII-beta) (CD16-I) (Fc-gamma RIII) (Fc-gamma RIIIb) (FcRIII) (FcRIIIb) (FcR-10) (IgG Fc receptor III-1) (CD antigen CD16b)
Protein function Receptor for the Fc region of immunoglobulins gamma. Low affinity receptor. Binds complexed or aggregated IgG and also monomeric IgG. Contrary to III-A, is not capable to mediate antibody-dependent cytotoxicity and phagocytosis. May serve as a t
PDB 1E4J , 1E4K , 1FNL , 1T83 , 1T89 , 6EAQ
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF13895 Ig_2 27 104 Immunoglobulin domain Domain
PF13895 Ig_2 108 190 Immunoglobulin domain Domain
Tissue specificity TISSUE SPECIFICITY: Expressed specifically by polymorphonuclear leukocytes (neutrophils). Also expressed by stimulated eosinophils.
Sequence
Sequence length 233
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Phagosome
Osteoclast differentiation
Neutrophil extracellular trap formation
Natural killer cell mediated cytotoxicity
Fc gamma R-mediated phagocytosis
Leishmaniasis
Staphylococcus aureus infection
Tuberculosis
Systemic lupus erythematosus
  Post-translational modification: synthesis of GPI-anchored proteins
Neutrophil degranulation
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
12
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
ANTI-CENTROMERE-ANTIBODY-POSITIVE SYSTEMIC SCLERODERMA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
DERMATITIS, ALLERGIC CONTACT CTD
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
GRANULOMATOSIS WITH POLYANGIITIS CTD
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
HYPERGLYCEMIA CTD
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Acute monocytic leukemia Monocytic Leukemia BEFREE 29862539
★☆☆☆☆
Found in Text Mining only
Acute pancreatitis Pancreatitis BEFREE 15599151
★☆☆☆☆
Found in Text Mining only
Addison Disease Addison`s Disease BEFREE 17523948
★☆☆☆☆
Found in Text Mining only
Adenocarcinoma Adenocarcinoma BEFREE 23441128
★☆☆☆☆
Found in Text Mining only
Adenocarcinoma of prostate Prostate adenocarcinoma BEFREE 23619475
★☆☆☆☆
Found in Text Mining only
Adrenoleukodystrophy Adrenoleukodystrophy Pubtator 21564078 Associate
★☆☆☆☆
Found in Text Mining only
Adult Diffuse Large B-Cell Lymphoma B-cell Lymphoma BEFREE 16609067, 17606457, 21667346, 21883784, 25050883, 27282998
★☆☆☆☆
Found in Text Mining only
Adult Hodgkin Lymphoma Hodgkin Lymphoma BEFREE 20423913, 24670809
★☆☆☆☆
Found in Text Mining only
Adult T-Cell Lymphoma/Leukemia T-Cell Lymphoma/Leukemia BEFREE 27091408
★☆☆☆☆
Found in Text Mining only
Adult type dermatomyositis Dermatomyositis BEFREE 19493236
★☆☆☆☆
Found in Text Mining only