Genes | GeDiPNet - Gene Disease Pathway & Associations

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All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

Showing genes starting with "F"

441 to 450 of 584 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
441	8061	FOSL1	FOS like 1, AP-1 transcription factor subunit	FRA, FRA1, fra-1	Asthma, Gout, Metabolic syndrome, Psoriasis, Diabetes mellitus type 2
442	2355	FOSL2	FOS like 2, AP-1 transcription factor subunit	ACED, FRA2	Aplasia cutis-enamel dysplasia syndrome, Juvenile arthritis, Asthma, Cardiovascular disease, Congenital scalp aplasia cutis-enamel hypoplasia-developmental delay-intellectual disability syndrome, Crohn disease, Glioblastoma, Inflammatory bowel disease, Juvenile idiopathic arthritis, Lung neoplasms, Neurodevelopmental disorder, Oligoarticular juvenile idiopathic arthritis, Diabetes mellitus type 1, Diabetes mellitus type 2, Ulcerative colitis
443	3169	FOXA1	Forkhead box A1	HNF3A, TCF3A	Breast neoplasms, Ductal carcinoma, Non-small-cell lung carcinoma, Squamous cell carcinoma, Fatty liver, Fatty liver, alcoholic, Prostatic neoplasms
444	3170	FOXA2	Forkhead box A2	HNF-3-beta, HNF3B, TCF3B	Combined pituitary hormone deficiency, Congenital hypopituitarism, Diabetes mellitus type 2, Liver cirrhosis, Lung disease
445	3171	FOXA3	Forkhead box A3	FKHH3, HNF3G, TCF3G	Asthma, Cholecystolithiasis, Coronary artery disease, Endometriosis, Gallstones, Inflammatory bowel disease, Osteoarthritis, Prostatic neoplasms, Respiratory system disease, Hypertension
446	27023	FOXB1	Forkhead box B1	FKH5, HFKH-5	Autism, Major depressive disorder, Obsessive-compulsive disorder, Diabetes mellitus type 2
447	442425	FOXB2	Forkhead box B2	FKH4, bA159H20.4	Astrocytoma, Kidney disease
448	2296	FOXC1	Forkhead box C1	ARA, ASGD3, FKHL7, FREAC-3, FREAC3, IGDA, IHG1, IRID1, RIEG3	Aniridia, Anterior segment dysgenesis, Anterior segment mesenchymal dysgenesis, Spinocerebellar ataxia, Axenfeld anomaly, Axenfeld-rieger syndrome, Congenital anomalies of the kidney and urinary tract, Cardiovascular disease, Coronary artery disease, Dandy-walker syndrome, Hypertension, Glaucoma, Iridogoniodysgenesis, Myocardial infarction, Prostatic neoplasms, Rieger syndrome, Tetralogy of fallot View all (2 more)
449	2303	FOXC2	Forkhead box C2	FKHL14, LD, MFH-1, MFH1	Blepharoptosis, Cardiovascular abnormalities, Congenital musculoskeletal anomalies, Craniofacial abnormalities, Diabetes mellitus type 2, Distichiasis-lymphedema syndrome, Eyelid disease, Non-immune hydrops fetalis, Hypertension, Lymphedema, Obesity, Tetralogy of fallot
450	2306	FOXD2	Forkhead box D2	FKHL17, FREAC-9, FREAC9	Androgenetic alopecia

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