Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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12881 to 12890 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

12881
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

12882
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

12883
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, Leprosy, Neurotic disorder, Biliary cholangitis, Prostate cancer, Systemic lupus erythematosus, Venous thromboembolism

12884
ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 5
SIAT8-E, SIAT8E, ST8SiaV
Major depressive disorder, Neurotic disorder, Prostate cancer, Scoliosis

12885
ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 6
SIA8F, SIAT8-F, SIAT8F, ST8SIA-VI, ST8SiaVI
Huntington disease, Hypertrophic cardiomyopathy

12886
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

12887
Stabilin 2
FEEL2, FELE-2, FELL2, FEX2, HARE, SCARH1
Hepatocellular carcinoma, Coronary artery disease, Prostatic neoplasms, Schizoaffective disorder, Scoliosis, Venous thromboembolism

12888
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

12889
SH3 and cysteine rich domain 2
24b2, 24b2/STAC2
Asthma, Moyamoya disease, Schizophrenia, Myopia

12890
SH3 and cysteine rich domain 3
CMYO13, CMYP13, MYPBB, NAM
Congenital myopathy, Hepatomegaly, Liver cirrhosis, Liver neoplasms, Native american myopathy