Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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12921 to 12930 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

12921
Striatin interacting protein 2
FAM40B, FAR11B
Tourette syndrome

12922
Small transmembrane regulator of ion transport 1
DWORF
Breast cancer, Estrogen-receptor negative breast cancer

12923
Striatin
PPP2R6A, SG2NA, STRN1
Basal cell carcinoma, Heart failure, Hypertrophic cardiomyopathy, Keratinocyte carcinoma, Metabolic syndrome, Schizophrenia, Diabetes mellitus type 2, Upper aerodigestive tract neoplasm

12924
Striatin 3
PPP2R6B, S/G2NA, SG2NA
Colorectal cancer

12925
Steroid sulfatase
ARSC, ARSC1, ASC, ES, SSDD, XLI
Rheumatoid arthritis, Attention deficit hyperactivity disorder, Autism, Fatty liver, Fatty liver, alcoholic, Alcoholic hepatitis, Diabetes mellitus type 2, Obesity, X-linked ichthyosis with steryl-sulfatase deficiency

12926
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

12927
STT3 oligosaccharyltransferase complex catalytic subunit B
CDG1X, SIMP, STT3-B
Graft versus host disease, Congenital disorder of glycosylation, Diabetic retinopathy, Gout, Schizophrenia

12928
STIP1 homology and U-box containing protein 1
CHIP, HSPABP2, NY-CO-7, SCA48, SCAR16, SDCCAG7, UBOX1
Spinocerebellar ataxia, Cerebellar ataxia

12929
Stum, mechanosensory transduction mediator homolog
C1orf95
Colonic neoplasms, Color vision deficiency, Diabetic retinopathy, Major depressive disorder, Proliferative diabetic retinopathy, Schizophrenia

12930
Syntaxin 10
SYN10, hsyn10
Ocular hypertension, Venous thromboembolism