Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
13021 to 13030 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

13021
SURP and G-patch domain containing 1
F23858, RBP, SF4
Atrial fibrillation, Cancer, Liver cirrhosis, Coronary artery disease, Diabetes mellitus, Diabetic eye disease, Heart failure, Liver neoplasms, Migraine, Nonalcoholic fatty liver disease, Stroke, Diabetes mellitus type 2

13022
SURP and G-patch domain containing 2
SFRS14, SRFS14
Hyperlipidemia

13023
SGT1 assembly cochaperone of MIS12 kinetochore complex
SGT1
Alzheimer disease

13024
Sulfatase 1
SULF-1
Autism, Cervical cancer, Crohn disease, Desbuquois syndrome, Inflammatory bowel disease, Ovarian neoplasms

13025
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

13026
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 neoplasms, Colonic neoplasms, Crohn disease, Inflammatory bowel disease, Insomnia, Myocardial ischemia, Neural tube defect, Neural tube defects, x-linked, Obesity, Prostatic neoplasms, Seasonal allergic rhinitis, Depression, Urologic neoplasms

13027
Sulfotransferase family 1A member 2
HAST4, P-PST, P-PST 2, ST1A2, STP2, TSPST2
Attention deficit hyperactivity disorder, Substance abuse

13028
Sulfotransferase family 1B member 1
ST1B1, ST1B2, SULT1B2
Autism, Central nervous system cancer, Glioblastoma, Glioma, Schizophrenia, Uterine fibroid

13029
Sulfotransferase family 1C member 2
ST1C1, ST1C2, SULT1C1, humSULTC2
Autism, Parkinson disease

13030
Sulfotransferase family 1C member 3
ST1C3
Autism