Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "S"

941 to 950 of 1203 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
941	6793	STK10	Serine/threonine kinase 10	LOK, PRO2729	Central nervous system cancer, Colorectal cancer, Crohn disease, Inflammatory bowel disease, Liver cirrhosis, Migraine, Ulcerative colitis
942	6794	STK11	Serine/threonine kinase 11	LKB1, PJS, hLKB1	Ankylosing spondylitis, Distal arthrogryposis, Pancreatic carcinoma, Squamous cell carcinoma, Crohn disease, Pancreatic cancer, Hypertension, Hypertrophy, Intestinal polyposis, Keratitis, Left ventricular disease, Lung neoplasms, Melanoma, Pancreatic neoplasm, Psoriasis View all (3 more)
943	6804	STX1A	Syntaxin 1A	HPC-1, P35-1, STX1, SYN1A	Autism, Neurodevelopmental disorder, Creutzfeldt-jakob disease, Cystic fibrosis, Hirschsprung disease, Intellectual developmental disorder, Neurodevelopmental disorders, Non-specific syndromic intellectual disability, Schizophrenia, Williams syndrome
944	6809	STX3	Syntaxin 3	DIAR12, MVID2, RDMVID, STX3A	Color vision deficiency, Microvillus inclusion disease
945	6811	STX5	Syntaxin 5	CDG2AA, SED5, STX5A	Congenital disorder of glycosylation
946	6812	STXBP1	Syntaxin binding protein 1	DEE4, MUNC18-1, N-Sec1, NSEC1, P67, RBSEC1, UNC18, unc-18A, unc18-1	Rett syndrome, Autism, Nonsyndromic intellectual disability, Cerebellar ataxia, Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay, Cryptogenic west syndrome, Developmental and epileptic encephalopathy, Developmental disability, Dravet syndrome, Myoclonic epilepsy, Epilepsy, Global developmental delay, Intellectual developmental disorder, Neurodevelopmental disorders, Pancreatitis View all (8 more)
947	6813	STXBP2	Syntaxin binding protein 2	FHL5, Hunc18b, MUNC18-2, UNC18-2, UNC18B, pp10122, unc-18B	Autoinflammatory syndrome, Platelet disorder, Carotid artery thrombosis, Hemophagocytic lymphohistiocytosis, Hemorrhage, Hereditary hemophagocytic lymphohistiocytosis, Microvillus inclusion disease, Mitochondrial complex deficiency
948	6817	SULT1A1	Sulfotransferase family 1A member 1	HAST1/HAST2, P-PST, P-PST 1, PST, ST1A1, ST1A3, STP, STP1, TSPST1, ts-PST	B-cell acute lymphoblastic leukemia, Breast neoplasm, Colonic neoplasm, Crohn disease, Inflammatory bowel disease, Insomnia, Myocardial ischemia, Neural tube defect, Obesity, Prostatic neoplasm, Seasonal allergic rhinitis, Depression
949	6820	SULT2B1	Sulfotransferase family 2B member 1	ARCI14, HSST2	Alzheimer disease, Astrocytoma, Autism, Cholelithiasis, Colorectal neoplasm, Congenital nonbullous ichthyosiform erythroderma, Endometrial neoplasm, Gallstones, Dermatomyositis, Lamellar ichthyosis, Prostatic neoplasm, Stroke
950	6821	SUOX	Sulfite oxidase	-	Ankylosing spondylitis, Asthma, Autism, Autoimmune disease, Autoimmune thyroid disease, Basal cell carcinoma, Celiac disease, Common variable immunodeficiency, Crohn disease, Gastroesophageal reflux disease, Juvenile idiopathic arthritis, Nasal polyp, Polycystic ovary syndrome, Psoriasis, Respiratory system disease View all (7 more)

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