Genesⓘ

Dataset:
? Protein-coding genes with reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "S"
1381 to 1390 of 1631 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1381
ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 5
SIAT8-E, SIAT8E, ST8SiaV
Major depressive disorder, Neurotic disorder, Prostate cancer, Scoliosis

1382
ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 6
SIA8F, SIAT8-F, SIAT8F, ST8SIA-VI, ST8SiaVI
Huntington disease, Hypertrophic cardiomyopathy

1383
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

1384
Stabilin 2
FEEL2, FELE-2, FELL2, FEX2, HARE, SCARH1
Hepatocellular carcinoma, Coronary artery disease, Prostatic neoplasm, Schizoaffective disorder, Scoliosis, Venous thromboembolism

1385
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

1386
SH3 and cysteine rich domain 2
24b2, 24b2/STAC2
Asthma, Moyamoya disease, Schizophrenia, Myopia

1387
SH3 and cysteine rich domain 3
CMYO13, CMYP13, MYPBB, NAM
Congenital myopathy, Hepatomegaly, Liver cirrhosis, Liver neoplasm, Native american myopathy

1388
STAG1 cohesin complex component
MRD47, SA1, SCC3A
Alzheimer disease, Anorexia nervosa, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Carpal tunnel syndrome, Neurodevelopmental disorder, Coronary artery disease, Dental caries, Global developmental delay, Intellectual developmental disorder, Major depressive disorder, Metabolic syndrome, Myocardial infarction, Myocardial ischemia
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1389
STAG2 cohesin complex component
HPE13, MKMS, NEDXCF, SA-2, SA2, SCC3B, bA517O1.1
Transitional cell carcinoma, Chromosome xq25 duplication syndrome, Holoprosencephaly, Myeloid leukemia, Myelodysplastic syndrome, Neurodevelopmental disorder, Semilobar holoprosencephaly, Urinary bladder neoplasms, Xq25 microduplication syndrome

1390
STAG3 cohesin complex component
SA3, SPGF61
Alzheimer disease, Major depressive disorder, Male infertility single gene azoospermia, Premature ovarian failure, Spermatogenic failure, Testicular azoospermia