Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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4611 to 4620 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

4611
Fc gamma receptor IIa
CD32, CD32A, CDw32, FCG2, FCGR2, FCGR2A1, FcGR, FcgammaRIIa, IGFR2
Hemolytic anemia, Ankylosing spondylitis, Rheumatoid arthritis, Atherosclerosis, Ischemic heart disease, Ulcerative colitis, Coronary artery disease, Crohn disease, Cystic fibrosis, Diffuse cutaneous systemic sclerosis, Epilepsy, Fetal erythroblastosis, Giant cell arteritis, Hemophilia a, Iga nephropathy
View all (14 more)

4612
Fc gamma receptor IIb
CD32, CD32B, FCG2, FCGR2, FCGR2C, FcGRIIB, FcRII-c, FcgammaRIIb, IGFR2
Ankylosing spondylitis, Systemic scleroderma, Autoimmune disease, Glomerulonephritis, Crest syndrome, Systemic lupus erythematosus, Neutropenia, Parkinson disease, Rheumatoid arthritis, Systemic sclerosis

4613
Fc gamma receptor IIc (gene/pseudogene)
CD32, CD32C, CDW32, FCG2, FCRIIC, FcgammaRIIc, IGFR2
Systemic lupus erythematosus, Diabetes mellitus type 2

4614
Fc gamma receptor IIIa
CD16, CD16-II, CD16A, FCG3, FCGR3, FCGRIII, FCR-10, FCRIII, FCRIIIA, FcGRIIIA, IGFR3, IMD20
Anti-glomerular basement membrane disease, Arthritis, Asthma, Rhinitis, Primary immunodeficiency with defective natural killer cell cytotoxicity, Behcet disease, Celiac disease, Ischemic heart disease, Coronary artery disease, Crohn disease, Epilepsy, Giant cell arteritis, Graft-versus-host disease, Iga nephropathy, Immunodeficiency
View all (10 more)

4615
Fc gamma receptor IIIb
CD16, CD16-I, CD16A, CD16b, FCG3, FCGR3, FCGR3A, FCR-10, FCRIII, FCRIIIb
Systemic scleroderma, Allergic contact dermatitis, Granulomatosis with polyangiitis, Hyperglycemia, Hyperinsulinism, Crest syndrome, Systemic lupus erythematosus, Lupus nephritis, Obesity, Parkinson disease, Systemic sclerosis

4616
Fc gamma receptor and transporter
FCRN, FcgammaRn, alpha-chain
Non-melanoma skin carcinoma, Diabetes mellitus type 2

4617
FCH and mu domain containing endocytic adaptor 1
IMD76
Color vision deficiency, Combined immunodeficiency disease, Coronary artery disease, Immunodeficiency, Myocardial infarction, Congenital neutropenia

4618
FCH and mu domain containing endocytic adaptor 2
-
Brain cancer, Brain neoplasms, Cholecystolithiasis, Coronary artery disease, Periodontal disease, Periodontitis, Small cell lung carcinoma, Venous thromboembolism

4619
FCH and double SH3 domains 2
NWK, NWK1, SH3MD3
Juvenile arthritis, Color vision deficiency, Crohn disease, Endometrial cancer, Inflammatory bowel disease, Insomnia, Irritable bowel syndrome, Juvenile idiopathic arthritis, Oligoarticular juvenile idiopathic arthritis, Psoriasis, Systemic lupus erythematosus, Diabetes mellitus type 2

4620
Ficolin 1
FCNM
Insomnia, Liver cirrhosis, Major depressive disorder, Post-traumatic stress disorder