Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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12531 to 12540 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

12531
Syntrophin alpha 1
LQT12, SNT1, TACIP1, dJ1187J4.5
Atrial fibrillation, Basal cell carcinoma, Becker muscular dystrophy, Breast cancer, Brugada syndrome, Cancer, Colorectal cancer, Dilated cardiomyopathy, Estrogen-receptor negative breast cancer, Long qt syndrome, Lung cancer, Melanoma, Myeloproliferative disorder, Non-melanoma skin carcinoma, Ovarian cancer
View all (7 more)

12532
Syntrophin beta 1
59-DAP, A1B, BSYN2, DAPA1B, SNT2, SNT2B1, TIP-43
Bipolar disorder, Colorectal cancer, Eosinophilia, Major depressive disorder, Osteosarcoma, Schizophrenia, Diabetes mellitus type 2

12533
Syntrophin beta 2
D16S2531E, EST25263, SNT2B2, SNT3, SNTL
Osteoarthritis, Schizophrenia

12534
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

12535
Syntrophin gamma 2
G2SYN, SYN5
Aortic stenosis, Aortic valve disease, Autism, Color vision deficiency, Dementia, Parenchymal hematoma, Schizophrenia, Myopia, Squamous cell carcinoma

12536
Sentan, cilia apical structure protein
S100A1L, S100AL, sentan
Atypical femoral fracture, Major depressive disorder

12537
Snurportin 1
KPNBL, LGMDR29, RNUT1, Snurportin1
Osteoarthritis, Diabetes mellitus type 2

12538
SNRPN upstream open reading frame
-
Angelman syndrome, Autism

12539
Sorting nexin 1
HsT17379, VPS5
Alzheimer disease

12540
Sorting nexin 10
OPTB8
Osteopetrosis, Dental caries, Desbuquois syndrome, Liver neoplasms, Metabolic syndrome, Diabetes mellitus type 2