Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "S"

1081 to 1090 of 1631 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
1081	22986	SORCS3	Sortilin related VPS10 domain containing receptor 3	SORCS	Alzheimer disease, Anorexia nervosa, Anxiety disorder, Atrial fibrillation, Attention deficit hyperactivity disorder, Autism, Behcet disease, Bipolar disorder, Breast cancer, Cardiovascular disease, Cerebral atherosclerosis, Neurodevelopmental disorder, Diabetic neuropathy, Gastroesophageal reflux disease, Hypertension View all (18 more)
1082	6652	SORD	Sorbitol dehydrogenase	HEL-S-95n, HMNR8, RDH, SDH, SORD1, SORDD, XDH	Alzheimer disease, Charcot-marie-tooth disease, Enterocolitis, Neuromuscular disease, Distal hereditary motor neuropathy
1083	6653	SORL1	Sortilin related receptor 1	C11orf32, LR11, LRP9, SORLA, SorLA-1, gp250	Alzheimer disease, Atrial fibrillation, Attention deficit hyperactivity disorder, Cannabis abuse, Cholelithiasis, Cognition disorder, Colorectal cancer, Hereditary spastic paraplegia, Dementia, Gastroesophageal reflux disease, Iga nephropathy, Insomnia, Mood disorder, Moyamoya angiopathy, Osteoarthritis View all (2 more)
1084	6272	SORT1	Sortilin 1	Gp95, LDLCQ6, NT3, NTR3	Alzheimer disease, Bipolar disorder, Cardiovascular disease, Cholelithiasis, Ischemic heart disease, Coronary artery disease, Liver disease, Major depressive disorder, Myocardial ischemia, Schizophrenia
1085	6654	SOS1	SOS Ras/Rac guanine nucleotide exchange factor 1	GF1, GGF1, GINGF, HGF, NS4, SOS-1	Atrial septal defect, Blepharoptosis, Brugada syndrome, Cafe-au-lait spots, Cardiofaciocutaneous syndrome, Dilated cardiomyopathy, Corticobasal degeneration, Costello syndrome, Desbuquois syndrome, Male infertility single gene azoospermia, Noonan syndrome, Tetralogy of fallot
1086	6655	SOS2	SOS Ras/Rho guanine nucleotide exchange factor 2	NS9, SOS-2	Cardiovascular disease, Kidney disease, Congenital malformation syndromes associated with short stature, Desbuquois syndrome, Hypertension, Gout, Kidney failure, Male infertility testicular dysgenesis, Noonan syndrome, Open angle glaucoma, Diabetes mellitus type 2
1087	50964	SOST	Sclerostin	CDD, DAND6, SOST1, VBCH	Bone fracture, Congenital cartilage disorder, Craniodiaphyseal dysplasia, Desbuquois syndrome, Osteochondrodysplasias, Bone dysplasia with increased bone density, Sclerosteosis, Van buchem disease
1088	25928	SOSTDC1	Sclerostin domain containing 1	CDA019, DAND7, ECTODIN, USAG1	Schizophrenia
1089	345079	SOWAHB	Sosondowah ankyrin repeat domain family member B	ANKRD56	Differentiated thyroid carcinoma, Hypertension, Thyroid carcinoma, Prostate cancer
1090	347454	SOWAHD	Sosondowah ankyrin repeat domain family member D	ANKRD58	Atrial fibrillation

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