Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "S"
531 to 540 of 1203 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

531
STAG3 cohesin complex component like 1 (pseudogene)
STAG3L1P, STAG3L2, STAG3L3

532
Spermine oxidase
C20orf16, PAO, PAO-1, PAO1, PAOH, PAOH1, SMO
Alzheimer disease, Androgenetic alopecia, Cerebrovascular disorder, Color vision deficiency, Dementia, Mood disorder, Panic disorder, Stroke

533
Shieldin complex subunit 2
FAM35A, FAM35A1, RINN2, bA163M19.1
Gout, Hyperinsulinemic hypoglycemia, Hyperinsulinism, Nephrolithiasis

534
Sidekick cell adhesion molecule 2
-
Alzheimer disease, Colorectal cancer, Dementia, Hepatitis b, Insomnia, Intellectual developmental disorder, Intestinal disease, Moyamoya disease, Myositis, Panic disorder, Polymyositis, Rheumatic disease, Senile cataract

535
SCAN domain containing 2 pseudogene
SCAND2

536
Solute carrier family 6 member 20
IMINO, SIT1, XT3, Xtrp3
Glycinuria with/without oxalate urolithiasis, Hirschsprung disease, Hyperglycinuria, Iminoglycinuria, Macular telangiectasia, Mesothelioma, Oligodendroglioma, Osteoarthritis

537
Sterile alpha motif domain containing 9
C7orf5, DRIF1, M7MLS2, MIRAGE, NFTC, OEF1, OEF2
Alzheimer disease, Androgenetic alopecia, Osteonecrosis of the femoral head, Intestinal disease, Myelodysplastic syndrome, Prostatic neoplasm, Spectrum and myeloid neoplasm risk, Schizophrenia, Tumoral calcinosis, Urogenital abnormalities

538
SID1 transmembrane family member 1
SID-1, SID1
Dental caries, Multiple sclerosis, Prostate cancer, Diabetes mellitus, type 2

539
SNF related kinase
HSNFRK
Asthma, Attention deficit hyperactivity disorder, Bipolar disorder, Colorectal cancer, Gastroesophageal reflux disease, Insomnia, Major depressive disorder, Intellectual developmental disorder, Obesity, Oligodendroglioma, Post-traumatic stress disorder, Schizophrenia, Substance abuse

540
Solute carrier family 66 member 1
LAAT-1, LAAT1, PQLC2
Hypothyroidism, Nephropathic cystinosis