Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "S"
221 to 230 of 1203 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

221
Solute carrier family 26 member 2
D5S1708, DTD, DTDST, EDM4, MST153, MSTP157
Achondrogenesis, Atelosteogenesis, Bone disease, Brachydactyly, Carnevale syndrome, Congenital cartilage disorder, Connective tissue disease, Craniofacial abnormalities, De la chapelle dysplasia, Desbuquois syndrome, Epiphyseal dysplasia, Juvenile idiopathic arthritis, Marshall syndrome, Osteochondrodysplasias, Oligoarticular juvenile idiopathic arthritis
View all (1 more)

222
Sphingosine-1-phosphate receptor 1
CD363, CHEDG1, D1S3362, ECGF1, EDG-1, EDG1, S1P1
Bipolar disorder, Carcinoma, Hypothyroidism, Liver cirrhosis

223
Secretory carrier membrane protein 5
-
Autism, Basal cell carcinoma, Neurodevelopmental disorder, Epilepsy, Global developmental delay, Intellectual developmental disorder, Neurodevelopmental disorders, Non-specific syndromic intellectual disability, Osteoarthritis, Systemic lupus erythematosus

224
Sperm associated antigen 17
CT143, PF6, SPGF55
Androgenetic alopecia, Breast cancer, Color vision deficiency, Craniodiaphyseal dysplasia, Eosinophilia, Male infertility single gene azoospermia, Meniere disease, Osteoarthritis, Scoliosis, Spermatogenic failure

225
Sprouty related EVH1 domain containing 2
NS14, Spred-2
Alzheimer disease, Anorexia nervosa, Aortic stenosis, Aortic valve disease, Rheumatoid arthritis, Attention deficit hyperactivity disorder, Coronary artery disease, Crohn disease, Desbuquois syndrome, Gout, Immune system disease, Inflammatory bowel disease, Lung cancer, Metabolic syndrome, Multiple sclerosis
View all (6 more)

226
Solute carrier family 51 member A
OSTA, OSTalpha, PFIC6, SLC51A1
Biliary cirrhosis, Cholelithiasis, Cognition disorder, Complications of diabetes mellitus, Delirium, dementia, and cognitive disorders, Diabetes complications, Liver cirrhosis, Biliary cholangitis, Progressive intrahepatic cholestasis

227
Solute carrier family 16 member 13
MCT13
Astrocytoma, Diabetes mellitus, type 2

228
Solute carrier family 39 member 11
C17orf26, ZIP-11, ZIP11
Alzheimer disease, Amyotrophic lateral sclerosis, Ankylosing spondylitis, Breast cancer, Crohn disease, Diverticular disease, Inflammatory bowel disease, Prostate cancer, Psoriasis, Sclerosing cholangitis, Diabetes mellitus, type 2, Ulcerative colitis

229
SPNS lysolipid transporter 3, sphingosine-1-phosphate (putative)
SLC62A3, SLC63A3
Clonal hematopoiesis, Coronary artery disease, Psychiatric disorders, Schizophrenia, Small cell lung carcinoma

230
STT3 oligosaccharyltransferase complex catalytic subunit B
CDG1X, SIMP, STT3-B
Graft versus host disease, Congenital disorder of glycosylation, Diabetic retinopathy, Gout, Schizophrenia