Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "S"
581 to 590 of 1203 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

581
Serine/threonine kinase 31
SGK396, TDRD8
Atypical femoral fracture, Colorectal cancer, Head and neck neoplasm, Human immunodeficiency virus infection, Insomnia, Alzheimer disease, Metabolic syndrome, Oropharyngeal cancer, Peripheral neuropathy, Schizophrenia, Diabetes mellitus, type 2, Upper aerodigestive tract neoplasm

582
Sushi domain containing 2
BK65A6.2, W5C5
Amyotrophic lateral sclerosis, Coronary artery disease

583
Solute carrier family 7 member 10
ASC1, HASC-1, asc-1
Alzheimer disease, Asthma, Eczema, B-cell acute lymphoblastic leukemia, Crohn disease, Hoarding disorder, Inflammatory bowel disease, Mastocytosis, Multiple sclerosis, Respiratory system disease, Schizophrenia, Seasonal allergic rhinitis, Ulcerative colitis

584
Solute carrier family 2 member 9
GLUT9, GLUTX, UAQTL2, URATv1
Alzheimer disease, Gouty arthritis, Attention deficit hyperactivity disorder, Cardiovascular disease, Kidney disease, Gout, Hyperuricemia, Ocular hypertension, Schizophrenia

585
SLC2A4 regulator
GEF, HDBP-1, HDBP1, Si-1-2, Si-1-2-19
Alzheimer disease, Asthma, Eczema, Gastroesophageal reflux disease, Multiple sclerosis, Prostate cancer

586
SLAM family member 8
BLAME, CD353, SBBI42
Crohn disease, Inflammatory bowel disease, Ulcerative colitis

587
Sphingosine kinase 2
SK 2, SK-2, SPK 2, SPK-2
Memory disorders, Psoriasis

588
StAR related lipid transfer domain containing 7
ADCME, BAFME2, FAME, FAME2, FCMTE2, GTT1
Familial adult myoclonic epilepsy, Benign adult familial myoclonic epilepsy

589
SNF2 related chromatin remodeling ATPase with DExD box 1
ADERM, BASNS, ETL1, HEL1, HRZ, TYS
Absence of fingerprints-congenital milia syndrome, Androgenetic alopecia, Atrial fibrillation, Bipolar disorder, Ectodermal dysplasia, Intellectual developmental disorder, Neurodevelopmental disorders, Prostatic neoplasm, Schizophrenia

590
SET and MYND domain containing 2
HSKM-B, KMT3C, ZMYND14
Alzheimer disease, Attention deficit hyperactivity disorder, Diverticular disease, Esophageal neoplasm, Gastroesophageal reflux disease, Major depressive disorder, Schizophrenia, Substance abuse