Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "S"
1371 to 1380 of 1624 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1371
Suppression of tumorigenicity 7 like
FAM4B, ST7R, STLR
Alzheimer disease, Open angle glaucoma, Pancreatic cancer

1372
ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1
GD3S, SIAT8, SIAT8-A, SIAT8A, ST8SiaI
Attention deficit hyperactivity disorder, Liver cirrhosis, Dementia, Liver disease, Major depressive disorder, Nonalcoholic fatty liver disease, Diabetes mellitus type 2

1373
ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2
HsT19690, SIAT8-B, SIAT8B, ST8SIA-II, ST8SiaII, STX
Autism, Bipolar disorder, Color vision deficiency, Colorectal cancer, Schizophrenia, Seasonal allergic rhinitis

1374
ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4
PST, PST1, SIAT8-D, SIAT8D, ST8SIA-IV, ST8SiaIV
Anxiety disorder, Biliary cirrhosis, Breast cancer, Color vision deficiency, Coronary artery disease, Crohn disease, Neurotic disorder, Biliary cholangitis, Prostate cancer, Systemic lupus erythematosus, Venous thromboembolism

1375
ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 5
SIAT8-E, SIAT8E, ST8SiaV
Major depressive disorder, Neurotic disorder, Prostate cancer, Scoliosis

1376
ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 6
SIA8F, SIAT8-F, SIAT8F, ST8SIA-VI, ST8SiaVI
Huntington disease, Hypertrophic cardiomyopathy

1377
Stabilin 1
CLEVER-1, FEEL-1, FEEL1, FELE-1, FEX1, HRFT, SCARH2, STAB-1
Juvenile arthritis, Bipolar disorder, Kidney disease, Gout, Hodgkin lymphoma, Hyperferritinemia, Juvenile idiopathic arthritis, Kidney failure, Major depressive disorder, Nephrolithiasis, Neurotic disorder, Oligoarticular juvenile idiopathic arthritis

1378
Stabilin 2
FEEL2, FELE-2, FELL2, FEX2, HARE, SCARH1
Hepatocellular carcinoma, Coronary artery disease, Prostatic neoplasms, Schizoaffective disorder, Scoliosis, Venous thromboembolism

1379
SH3 and cysteine rich domain
STAC1
Asthma, Brain aneurysm, Celiac disease, Kidney disease, Allergic contact dermatitis, Diabetic neuropathy, Generalized epilepsy, Immune system disease, Obesity, Scoliosis

1380
SH3 and cysteine rich domain 2
24b2, 24b2/STAC2
Asthma, Moyamoya disease, Schizophrenia, Myopia