Genes | GeDiPNet - Gene Disease Pathway & Associations

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5021 to 5030 of 15380 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
5021	283431	GAS2L3	Growth arrest specific 2 like 3	G2L3	Central nervous system cancer, Glioblastoma, Glioma
5022	2621	GAS6	Growth arrest specific 6	AXLLG, AXSF	Anorectal malformation, Adenoid cystic carcinoma, Cardiomegaly, Diabetic neuropathy, Hyperlipidemia, Kidney failure, Oligodendroglioma, Salivary gland neoplasms, Thromboembolism, Thrombosis
5023	8522	GAS7	Growth arrest specific 7	-	Kidney disease, Glaucoma, Obesity, Open angle glaucoma, Parkinson disease, Schizophrenia
5024	729085	GASK1A	Golgi associated kinase 1A	C3orf41, FAM198A	Breast cancer, Insomnia, Osteoarthritis
5025	51313	GASK1B	Golgi associated kinase 1B	AD021, AD036, C4orf18, ENED, FAM198B	Central nervous system cancer, Glioblastoma, Glioma
5026	2520	GAST	Gastrin	GAS	Barrett esophagus, Colonic neoplasms, Digestive system disease, Duodenal ulcer, Gastrointestinal disease, Lung neoplasms, Peptic ulcer disease, Stomach neoplasms
5027	2623	GATA1	GATA binding protein 1	CNSHA9, ERYF1, GATA-1, GF-1, GF1, HAEADA, NF-E1, NFE1, XLANP, XLTDA, XLTT	Anemia, Congenital nonspherocytic hemolytic anemia, Diamond-blackfan anemia, Anemia, x-linked, Beta thalassemia, Congenital erythropoietic porphyria, Cutaneous porphyria, Down syndrome, Dyserythropoietic anemia with thrombocytopenia, Hemolytic anemia, Major depressive disorder, Myelodysplastic syndrome, Porphyria, Thrombocytopenia, Thrombocytopenia with dyserythropoietic anemia View all (2 more)
5028	2624	GATA2	GATA binding protein 2	DCML, IMD21, MONOMAC, NFE1B	Myeloid leukemia, Anemia, Arteriosclerosis, Cardiovascular abnormalities, Cartilage disease, Clonal hematopoiesis, Craniofacial abnormalities, Deafness-lymphedema-leukemia syndrome, Gata2 deficiency, Immunodeficiency, Lymphedema, Major depressive disorder, Myelodysplastic syndrome, Primary graft dysfunction, Vascular remodeling, Vasculitis View all (1 more)
5029	2625	GATA3	GATA binding protein 3	HDR, HDRS	Rheumatoid arthritis, Asthma, Eczema, Autoimmune disease, Barakat syndrome, B-cell acute lymphoblastic leukemia, B-lymphoblastic leukemia/lymphoma, Congenital anomalies of the kidney and urinary tract, Carcinogenesis, Carcinoma, Kidney disease, Colorectal cancer, Eosinophilia, Gastro-entero-pancreatic neuroendocrine tumor, Hearing impairment View all (16 more)
5030	2626	GATA4	GATA binding protein 4	ASD2, TACHD, TOF, VSD1	46,xy partial gonadal dysgenesis, Alzheimer disease, Asthma, Atrial fibrillation, Atrial septal defect, Atrioventricular septal defect, Brugada syndrome, Cardiomegaly, Dilated cardiomyopathy, Cholecystolithiasis, Chromosome 8p23.1 monosomy, Colorectal neoplasms, Congenital pulmonary valve atresia, Congenital heart defects, Congenital heart disease View all (31 more)

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