Genes | GeDiPNet - Gene Disease Pathway & Associations

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5031 to 5040 of 15380 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
5031	140628	GATA5	GATA binding protein 5	CHTD5, GATAS, bB379O24.1	Aortic valve disease, Atrial fibrillation, Benign prostatic hyperplasia, Bicuspid aortic valve, Dilated cardiomyopathy, Central serous retinopathy, Obstructive pulmonary disease, Colorectal neoplasms, Congenital heart disease, Thoracic aortic aneurysm and aortic dissection, Hereditary atrial fibrillation, Hypertension, Kidney cancer, Prostate cancer, Tetralogy of fallot View all (3 more)
5032	2627	GATA6	GATA binding protein 6	-	Atrial septal defect, Atrioventricular septal defect, Benign prostatic hyperplasia, Dilated cardiomyopathy, Obstructive pulmonary disease, Common arterial trunk with aortic dominance, Common arterial trunk with pulmonary dominance and interrupted aortic arch, Congenital diaphragmatic hernia, Congenital heart defects, Conotruncal cardiac defect, Developmental disability, Endometrial cancer, Endometrial neoplasms, Atrial fibrillation, Congenital heart defect View all (13 more)
5033	57798	GATAD1	GATA zinc finger domain containing 1	CMD2B, ODAG, RG083M05.2	Dilated cardiomyopathy, Color vision deficiency, Heimler syndrome, Optic atrophy, Peroxisome biogenesis disorder
5034	54815	GATAD2A	GATA zinc finger domain containing 2A	p66alpha	Alzheimer disease, Anorexia nervosa, Atrial fibrillation, Attention deficit hyperactivity disorder, Breast cancer, Diabetes mellitus, Dyslexia, Estrogen-receptor negative breast cancer, Gastroesophageal reflux disease, Genetic predisposition to disease, Insomnia, Intrahepatic bile duct cancer, Liver cancer, Liver neoplasms, Neurodevelopmental disorder View all (7 more)
5035	57459	GATAD2B	GATA zinc finger domain containing 2B	GANDS, MRD18, P66beta, p68	Androgenetic alopecia, Eczema, Attention deficit hyperactivity disorder, Autism, Conduct disorder, Intellectual developmental disorder, Prostate cancer, Intellectual disability
5036	5188	GATB	Glutamyl-tRNA amidotransferase subunit B	COXPD41, HSPC199, PET112, PET112L	Alzheimer disease, Attention deficit hyperactivity disorder, Autism, Combined oxidative phosphorylation deficiency, Dementia, Large artery stroke
5037	283459	GATC	Glutamyl-tRNA amidotransferase subunit C	15E1.2, COXPD42	Combined oxidative phosphorylation deficiency, Scoliosis
5038	347862	GATD1	Glutamine amidotransferase class 1 domain containing 1	FERRY5, Fy-5, PDDC1	Fuchs endothelial dystrophy
5039	8209	GATD3	Glutamine amidotransferase class 1 domain containing 3	C21orf33, ES1, GATD3A, GATD3B, GT335, HES1, KNPH, KNPI	Ankylosing spondylitis, Anophthalmia/microphthalmia-esophageal atresia syndrome, Celiac disease, Crohn disease, Inflammatory bowel disease, Psoriasis, Sclerosing cholangitis, Diabetes mellitus type 1, Diabetes mellitus type 2, Ulcerative colitis
5040	2628	GATM	Glycine amidinotransferase	AGAT, AT, CCDS3, FRTS, FRTS1, RFS	Agat deficiency, Arginine-glycine amidinotransferase deficiency, Carcinoma, Cerebral creatine deficiency syndrome, Kidney disease, Congestive heart failure, De toni-debre-fanconi syndrome, Fanconi renotubular syndrome, Fanconi syndrome, Heart failure, Kidney failure, Lennox-gastaut syndrome, Myocardial ischemia, Necrosis

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