Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "S"
1031 to 1040 of 1631 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1031
Syntrophin gamma 1
G1SYN, SYN4
Attention deficit hyperactivity disorder, Breast cancer, Color vision deficiency, Gastroparesis, Hypertension, Ovarian epithelial cancer, Obstructive sleep apnea syndrome, Ovarian cancer, Scoliosis, Substance abuse, Diabetes mellitus type 2

1032
Syntrophin gamma 2
G2SYN, SYN5
Aortic stenosis, Aortic valve disease, Autism, Color vision deficiency, Dementia, Parenchymal hematoma, Schizophrenia, Myopia, Squamous cell carcinoma

1033
Sentan, cilia apical structure protein
S100A1L, S100AL, sentan
Atypical femoral fracture, Major depressive disorder

1034
Snurportin 1
KPNBL, LGMDR29, RNUT1, Snurportin1
Osteoarthritis, Diabetes mellitus type 2

1035
SNRPN upstream open reading frame
-
Angelman syndrome, Autism

1036
Sorting nexin 1
HsT17379, VPS5
Alzheimer disease

1037
Sorting nexin 10
OPTB8
Osteopetrosis, Dental caries, Desbuquois syndrome, Liver neoplasms, Metabolic syndrome, Diabetes mellitus type 2

1038
Sorting nexin 11
-
Anorexia nervosa, Atrial fibrillation, Endometrial cancer, Endometrial neoplasms, Schizophrenia, Diabetes mellitus type 2

1039
Sorting nexin 13
RGS-PX1
Basal cell carcinoma, Color vision deficiency, Coronary artery disease, Keratinocyte carcinoma, Metabolic syndrome, Parkinson disease, Diabetes mellitus type 2, Ulcerative colitis, Venous thromboembolism

1040
Sorting nexin 14
RGS-PX2, SCAR20
Spinocerebellar ataxia, Cerebellar ataxia, Global developmental delay, Intellectual developmental disorder, Intellectual developmental disorder dysmorphic cerebellar, Neurodevelopmental disorder