Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "S"
321 to 330 of 1203 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

321
Solute carrier family 39 member 6
LIV-1, LIV1, ZIP6
Breast neoplasm, Esophageal cancer, Esophageal squamous cell carcinoma, Liver cirrhosis, Squamous cell carcinoma

322
SAM pointed domain containing ETS transcription factor
PDEF, bA375E1.3
Lymphocytic leukemia, Crohn disease, Inflammatory bowel disease, Insomnia, Ovarian neoplasm, Prostate cancer, Diabetes mellitus, type 2, Ulcerative colitis

323
SAMM50 sorting and assembly machinery component
CGI-51, OMP85, SAM50, TOB55, TRG-3, YNL026W
Attention deficit hyperactivity disorder, Gout, Hepatocellular carcinoma, Hypogonadism, Nonalcoholic fatty liver disease, Schizophrenia, Diabetes mellitus, type 2

324
Sulfotransferase family 4A member 1
BR-STL-1, BRSTL1, DJ388M5.3, NST, SULTX3, hBR-STL-1
Schizoaffective disorder, Schizophrenia, Diabetes mellitus, type 2

325
SAM and HD domain containing deoxynucleoside triphosphate triphosphohydrolase 1
CHBL2, DCIP, HDDC1, MOP-5, SBBI88, hSAMHD1
Aicardi goutieres syndrome, Alzheimer disease, Cerebral palsy, Chilblain lupus erythematosus, Deoxyguanosine kinase deficiency, Diabetic neuropathy, Chilblain lupus, Hepatitis b, Hepatitis c, Moyamoya disease, Interferonopathy

326
SIN3 transcription regulator family member A
CHR15DELq24, DEL15Q24, WITKOS
15q14 microdeletion syndrome, Autism, Breast cancer, Chromosome 15q24 deletion syndrome, Craniofacial abnormalities, Gout, Hydrocephalus, Intellectual developmental disorder, Microcephaly, Neurodevelopmental disorders, Diabetes mellitus, type 2, Witteveen-kolk syndrome

327
SH2B adaptor protein 1
PSM, SH2B
Chromosome 16p11.2 deletion syndrome, Crohn disease, Chromosome 16p11.2 microdeletion syndrome, Inflammatory bowel disease, Obesity, Premature ovarian failure, Schizophrenia, Ulcerative colitis

328
Sushi, nidogen and EGF like domains 1
IRE-BP1, SST3, Snep

329
Spermatogenesis associated serine rich 2 like
DNAPTP6, SGNP
Aortic disease, Atrial fibrillation, Atrial flutter, Attention deficit hyperactivity disorder, Bipolar disorder, Obstructive pulmonary disease, Crohn disease, Dilated cardiomyopathy, Esophageal disease, Esophageal ulcer, Heart failure, Hypertrophic cardiomyopathy, Inflammatory bowel disease, Insomnia, Metabolic syndrome
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330
Signal induced proliferation associated 1 like 1
E6TP1, SPAR1
Juvenile arthritis, Autism, Breast benign neoplasm, Color vision deficiency, Heart failure, Hypertension, Hypertrophic cardiomyopathy, Juvenile idiopathic arthritis, Myocardial infarction, Neurotic disorder, Obesity, Oligodendroglioma, Otosclerosis, Oligoarticular juvenile idiopathic arthritis, Pulmonary edema
View all (1 more)