FCGR1A (Fc gamma receptor Ia)

Gene Gene information from NCBI Gene database.
Gene miRNA Transcription factors Gene ontology Other IDs Protein Pathways Associated diseases
Entrez ID 2209
Gene name Fc gamma receptor Ia
Gene symbol FCGR1A
Synonyms (NCBI Gene)
CD64CD64AFCG1FCGR1FCRIFcgammaRIIGFR1
Chromosome 1
Chromosome location 1q21.2
Summary This gene encodes a protein that plays an important role in the immune response. This protein is a high-affinity Fc-gamma receptor. The gene is one of three related gene family members located on chromosome 1. [provided by RefSeq, Jul 2008]
miRNA miRNA information provided by mirtarbase database.
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Gene miRNA Transcription factors Gene ontology Other IDs Protein Pathways Associated diseases
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miRTarBase ID miRNA Experiments Reference
MIRT993836 hsa-miR-3120-5p CLIP-seq
MIRT993837 hsa-miR-4311 CLIP-seq
MIRT993838 hsa-miR-4652-3p CLIP-seq
MIRT993839 hsa-miR-4711-3p CLIP-seq
MIRT993840 hsa-miR-4753-3p CLIP-seq
Transcription factors Transcription factors information provided by TRRUST V2 database.
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Transcription factor Regulation Reference
SPI1 Unknown 10820245;14734612
STAT1 Unknown 14734612
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
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GO ID Ontology Definition Evidence Reference
GO:0001788 Process Antibody-dependent cellular cytotoxicity IBA
GO:0001788 Process Antibody-dependent cellular cytotoxicity IDA 11711607
GO:0001788 Process Antibody-dependent cellular cytotoxicity IEA
GO:0001788 Process Antibody-dependent cellular cytotoxicity IEA
GO:0001798 Process Positive regulation of type IIa hypersensitivity IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
Gene miRNA Transcription factors Gene ontology Other IDs Protein Pathways Associated diseases
MIM HGNC e!Ensembl
146760 3613 ENSG00000150337
Protein Protein information from UniProt database.
Gene miRNA Transcription factors Gene ontology Other IDs Protein Pathways Associated diseases
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P12314
Protein name High affinity immunoglobulin gamma Fc receptor I (IgG Fc receptor I) (Fc-gamma RI) (FcRI) (Fc-gamma RIA) (FcgammaRIa) (CD antigen CD64)
Protein function High affinity receptor for the Fc region of immunoglobulins gamma. Functions in both innate and adaptive immune responses. Mediates IgG effector functions on monocytes triggering antibody-dependent cellular cytotoxicity (ADCC) of virus-infected
PDB 3RJD , 4W4O , 4X4M , 4ZNE , 8DIN , 8DIR , 8DJ7
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF13927 Ig_3 23 → 87 Domain
PF13895 Ig_2 104 → 185 Immunoglobulin domain Domain
PF00047 ig 195 → 275 Immunoglobulin domain Domain
Tissue specificity TISSUE SPECIFICITY: Monocyte/macrophage specific.
Sequence
Sequence length 374
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
Gene miRNA Transcription factors Gene ontology Other IDs Protein Pathways Associated diseases
  KEGG  Reactome
  Phagosome
Osteoclast differentiation
Neutrophil extracellular trap formation
Hematopoietic cell lineage
Fc gamma R-mediated phagocytosis
Leishmaniasis
Staphylococcus aureus infection
Tuberculosis
Transcriptional misregulation in cancer
Acute myeloid leukemia
Systemic lupus erythematosus 		  Cross-presentation of soluble exogenous antigens (endosomes)
Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell
FCGR activation
Regulation of actin dynamics for phagocytic cup formation
Role of phospholipids in phagocytosis
Interferon gamma signaling
FCGR3A-mediated IL10 synthesis
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
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Gene miRNA Transcription factors Gene ontology Other IDs Protein Pathways Associated diseases
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Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
FCGR1A-related disorder Uncertain significance rs74315310 RCV005394164
IGG receptor I, phagocytic, familial deficiency of Uncertain significance rs74315310 RCV000015950
Nonpapillary renal cell carcinoma Uncertain significance rs74315310 RCV005887528
Peritoneal Gliomatosis Uncertain significance rs637882 RCV000852293
Show/Hide Text Mining Associations (148)
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Acquired Immunodeficiency Syndrome Associate 10931386
Agammaglobulinemia Associate 26708396
AIDS Associated Nephropathy Associate 23982074
Alzheimer Disease Associate 30193587, 33186918, 34602489
Anaphylaxis Associate 30189430
Anemia Sickle Cell Associate 9414294
Arthritis Associate 22251373
Arthritis Infectious Stimulate 32849606
Arthritis Juvenile Stimulate 30683706
Arthritis Juvenile Associate 32849606