Genesⓘ

Dataset:
? Protein-coding genes with reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "S"
1461 to 1470 of 1631 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1461
Stonin 1
SALF, SBLF, STN1, STNB1
Post-operative atrial fibrillation, Amyotrophic lateral sclerosis

1462
STON1-GTF2A1L readthrough
ALF, GTF2A1L, GTF2A1LF, SALF
Testotoxicosis, Hypertrophic cardiomyopathy, Metabolic syndrome, Polycystic ovary syndrome, Post-operative atrial fibrillation, Hypogonadism, Amyotrophic lateral sclerosis, Diabetes mellitus, type 2

1463
Stonin 2
STN2, STNB, STNB2
Obesity, Schizophrenia

1464
Storkhead box 1
C10orf24
Atrial fibrillation, Cervical cancer, Insomnia, Preeclampsia, Schizophrenia

1465
Storkhead box 2
-
Androgenetic alopecia, Differentiated thyroid carcinoma, Major depressive disorder, Mood disorder, Obesity, Open angle glaucoma, Sarcoidosis

1466
Sperm tail PG-rich repeat containing 1
C1orf201, MAPO2
Prostate cancer, Van der woude syndrome

1467
Sperm tail PG-rich repeat containing 2
C4orf37
Aortic stenosis, Aortic valve disease, Attention deficit hyperactivity disorder, Breast cancer, Bronchial disease, Color vision deficiency, Scoliosis, Substance abuse

1468
Sperm-tail PG-rich repeat containing 4
C2orf61, GSE
Alzheimer disease, Color vision deficiency, Dementia

1469
Signaling receptor and transporter of retinol STRA6
MCOPCB8, MCOPS9, PP14296, SLC69A1
Anophthalmia, Anophthalmia/microphthalmia-esophageal atresia syndrome, Cardiovascular abnormalities, Central nervous system cancer, Colobomatous microphthalmia, Congenital heart disease, Craniofacial abnormalities, Glioblastoma, Glioma, Congenital heart defect, Intellectual developmental disorder, Lung disease, Microphthalmia, Microphthalmos

1470
Stimulated by retinoic acid 8
-
Male infertility single gene azoospermia