Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "S"
811 to 820 of 1203 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

811
Solute carrier family 18 member A3
CMS21, VACHT
Presynaptic congenital myasthenic syndromes, Congenital myasthenic syndrome, Fetal akinesia deformation sequence, Hodgkin lymphoma, Myasthenic syndrome, Pena-shokeir syndrome type i, Presynaptic congenital myasthenic syndrome

812
Solute carrier family 19 member 1
CHMD, FOLT, IFC-1, IFC1, IMD114, MEGAF, REFC, RFC, RFC1, RFT-1, hRFC, hSLC19A1
Autism, Cataract, Colonic neoplasm, Colorectal neoplasm, Combined immunodeficiency, Down syndrome, Glaucoma, Immunodeficiency, Knobloch syndrome, Macular dystrophy, Megaloblastic anemia, Nervous system disease, Nystagmus, Retinitis pigmentosa, Myopia
View all (1 more)

813
Solute carrier family 20 member 1
GLVR1, Glvr-1, PIT1, PiT-1
Aortic valve disease, Bone disease, Endometriosis, Liver cirrhosis, Metabolic bone disorder

814
Solute carrier family 20 member 2
GLVR-2, GLVR2, IBGC1, IBGC2, IBGC3, MLVAR, PIT-2, PIT2, RAM1, Ram-1
Idiopathic basal ganglia calcification, Basal ganglia disease, Primary familial brain calcification, Calcinosis, Vascular dementia, Fahr's disease, Gout, Respiratory system disease, Tonsillitis

815
Solute carrier family 25 member 1
CIC, CMS23, CTP, D2L2AD, SEA, SLC20A3
Combined d-2- and l-2-hydroxyglutaric aciduria, Combined d-2-hydroxyglutaric aciduria and l-2-hydroxyglutaric aciduria, Presynaptic congenital myasthenic syndromes, Congenital myasthenic syndrome, D-2-hydroxyglutaric aciduria, Mitochondrial disease, Myasthenic syndrome, Presynaptic congenital myasthenic syndrome

816
Solute carrier organic anion transporter family member 2A1
MATR1, OATP2A1, PGT, PHOAD, PHOAR2, SLC21A2
Autism, Basal cell carcinoma, Enteropathy, Colorectal adenoma, Colorectal cancer, Colorectal neoplasm, Desbuquois syndrome, Primary hypertrophic osteoarthropathy , Inflammatory bowel disease, Primary hypertrophic osteoarthropathy

817
Solute carrier organic anion transporter family member 1A2
OATP, OATP-A, OATP1A2, SLC21A3
Asthma, Cholelithiasis, Myopathy, Progressive supranuclear palsy

818
Solute carrier family 22 member 1
HOCT1, OCT1, oct1_cds
Hepatocellular carcinoma, Colonic neoplasm, Color vision deficiency, Coronary artery disease, Hypertension, Gout, Hirschsprung disease, Myocardial infarction, Obesity, Prostate cancer

819
Solute carrier family 22 member 3
EMT, EMTH, OCT3
Barrett esophagus, Breast cancer, Cancer, Cardiovascular disease, Hepatitis c virus infection, Colorectal cancer, Coronary artery disease, Diabetes mellitus type 2, Esophageal adenocarcinoma, Estrogen-receptor negative breast cancer, Hyperlipidemia, Gout, Lung cancer, Metabolic syndrome, Myocardial infarction
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820
Solute carrier family 22 member 2
Oct-02
Barrett esophagus, Bladder calculus, Cardiovascular disease, Kidney disease, Coronary artery disease, Esophageal adenocarcinoma, Hyperlipidemia, Hypertensive nephropathy, Kidney failure, Major depressive disorder, Intellectual developmental disorder, Metabolic syndrome, Myocardial infarction, Nephrolithiasis, Obesity
View all (7 more)