Genesⓘ

Dataset:
? Protein-coding genes with reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "S"
1521 to 1530 of 1631 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1521
Sulfatase 1
SULF-1
Autism, Cervical cancer, Crohn disease, Desbuquois syndrome, Inflammatory bowel disease, Ovarian neoplasm

1522
Sulfatase 2
HSULF-2
Androgenetic alopecia, Atrial fibrillation, Attention deficit hyperactivity disorder, Autism, Central nervous system cancer, Endometriosis, Glioma, Metabolic syndrome, Oligodendroglioma, Osteoarthritis, Sarcoidosis, Diabetes mellitus, type 2

1523
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, Neural tube defects, x-linked, Obesity, Prostatic neoplasm, Seasonal allergic rhinitis, Depression, Urologic neoplasm

1524
Sulfotransferase family 1A member 2
HAST4, P-PST, P-PST 2, ST1A2, STP2, TSPST2
Attention deficit hyperactivity disorder, Substance abuse

1525
Sulfotransferase family 1B member 1
ST1B1, ST1B2, SULT1B2
Autism, Central nervous system cancer, Glioblastoma, Glioma, Schizophrenia, Uterine fibroid

1526
Sulfotransferase family 1C member 2
ST1C1, ST1C2, SULT1C1, humSULTC2
Autism, Parkinson disease

1527
Sulfotransferase family 1C member 3
ST1C3
Autism

1528
Sulfotransferase family 1E member 1
EST, EST-1, ST1E1, STE
Central nervous system cancer, Chondromalacia, Glioblastoma, Glioma, Alcoholic hepatitis, Liver cirrhosis, Liver disease, Prostatic neoplasm, Uterine fibroid

1529
Sulfotransferase family 2A member 1
DHEA-ST, DHEA-ST8, DHEAS, HST, ST2, ST2A1, ST2A3, STD, SULT2A3, hSTa
Cholecystolithiasis, Gallstones, Intrahepatic cholestasis of pregnancy, Liver cirrhosis, Peripheral vascular disease, Prostatic neoplasm, Vascular disease

1530
Sulfotransferase family 2B member 1
ARCI14, HSST2
Alzheimer disease, Astrocytoma, Autism, Cholelithiasis, Colorectal neoplasm, Congenital ichthyosiform erythroderma, Congenital nonbullous ichthyosiform erythroderma, Endometrial neoplasm, Gallstones, Dermatomyositis, Lamellar ichthyosis, Prostatic neoplasm, Stroke