Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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12471 to 12480 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

12471
Small nuclear ribonucleoprotein polypeptide N
HCERN3, PWCR, RT-LI, SM-D, SMN, SNRNP-N, SNURF-SNRPN, sm-N
Angelman syndrome, Autism, Obesity, Prader-willi syndrome, Prostate cancer

12472
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)

12473
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

12474
Syntrophin beta 2
D16S2531E, EST25263, SNT2B2, SNT3, SNTL
Osteoarthritis, Schizophrenia

12475
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

12476
Syntrophin gamma 2
G2SYN, SYN5
Aortic stenosis, Aortic valve disease, Autism, Color vision deficiency, Dementia, Parenchymal hematoma, Schizophrenia, Myopia, Squamous cell carcinoma

12477
Sentan, cilia apical structure protein
S100A1L, S100AL, sentan
Atypical femoral fracture, Major depressive disorder

12478
Snurportin 1
KPNBL, LGMDR29, RNUT1, Snurportin1
Osteoarthritis, Diabetes mellitus type 2

12479
SNRPN upstream open reading frame
-
Angelman syndrome, Autism

12480
Sorting nexin 1
HsT17379, VPS5
Alzheimer disease