Genesⓘ

Dataset:
? Protein-coding genes with reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "S"
1481 to 1490 of 1631 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1481
412
STS
Steroid sulfatase
ARSC, ARSC1, ASC, ES, SSDD, XLI
Rheumatoid arthritis, Attention deficit hyperactivity disorder, Autism, Experimental diabetes, Fatty liver, Fatty liver, alcoholic, Alcoholic hepatitis, Diabetes mellitus, type 2, Obesity, X-linked ichthyosis with steryl-sulfatase deficiency

1482
STT3 oligosaccharyltransferase complex catalytic subunit A
CDG1WAD, CDG1WAR, ITM1, STT3-A, TMC
Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Congenital disorder of glycosylation, Major depressive disorder, Schizophrenia

1483
STT3 oligosaccharyltransferase complex catalytic subunit B
CDG1X, SIMP, STT3-B
Graft versus host disease, Congenital disorder of glycosylation, Diabetic retinopathy, Gout, Schizophrenia

1484
STIP1 homology and U-box containing protein 1
CHIP, HSPABP2, NY-CO-7, SCA48, SCAR16, SDCCAG7, UBOX1
Spinocerebellar ataxia, Cerebellar ataxia

1485
Stum, mechanosensory transduction mediator homolog
C1orf95
Colonic neoplasm, Color vision deficiency, Diabetic retinopathy, Major depressive disorder, Proliferative diabetic retinopathy, Schizophrenia

1486
Syntaxin 10
SYN10, hsyn10
Ocular hypertension, Venous thromboembolism

1487
Syntaxin 11
FHL4, HLH4, HPLH4
Autoinflammatory syndrome, Disorder of development or morphogenesis, Hemophagocytic lymphohistiocytosis, Hereditary hemophagocytic lymphohistiocytosis, Scoliosis

1488
Syntaxin 12
STX13, STX14
Diabetes mellitus, type 2

1489
Syntaxin 16
SYN-16, SYN16
Pseudohypoparathyroidism

1490
Syntaxin 17
-
Insomnia, Melanoma