Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "F"
251 to 260 of 580 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

251
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

252
Fc gamma receptor IIc (gene/pseudogene)
CD32, CD32C, CDW32, FCG2, FCRIIC, FcgammaRIIc, IGFR2
Systemic lupus erythematosus, Diabetes mellitus type 2

253
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
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254
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

255
Fc gamma receptor and transporter
FCRN, FcgammaRn, alpha-chain
Non-melanoma skin carcinoma, Diabetes mellitus type 2

256
FCH and mu domain containing endocytic adaptor 1
IMD76
Color vision deficiency, Combined immunodeficiency disease, Coronary artery disease, Immunodeficiency, Myocardial infarction, Congenital neutropenia

257
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

258
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

259
Ficolin 1
FCNM
Insomnia, Major depressive disorder, Post-traumatic stress disorder

260
Ficolin 2
EBP-37, FCNL, P35, ficolin-2
Alzheimer disease, Hepatocellular carcinoma, Mesothelioma, Oligodendroglioma, Thyrotoxic periodic paralysis