Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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12821 to 12830 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

12821
Suppression of tumorigenicity 7 like
FAM4B, ST7R, STLR
Alzheimer disease, Open angle glaucoma, Pancreatic cancer

12822
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

12823
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

12824
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

12825
ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 5
SIAT8-E, SIAT8E, ST8SiaV
Major depressive disorder, Neurotic disorder, Prostate cancer, Scoliosis

12826
ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 6
SIA8F, SIAT8-F, SIAT8F, ST8SIA-VI, ST8SiaVI
Huntington disease, Hypertrophic cardiomyopathy

12827
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

12828
Stabilin 2
FEEL2, FELE-2, FELL2, FEX2, HARE, SCARH1
Hepatocellular carcinoma, Coronary artery disease, Prostatic neoplasms, Schizoaffective disorder, Scoliosis, Venous thromboembolism

12829
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

12830
SH3 and cysteine rich domain 2
24b2, 24b2/STAC2
Asthma, Moyamoya disease, Schizophrenia, Myopia