Genesⓘ

Dataset:
? Protein-coding genes with reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "S"
601 to 610 of 1631 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

601
Solute carrier family 22 member 10 (gene/pseudogene)
OAT5, hOAT5
Hepatocellular carcinoma, Non-small-cell lung carcinoma, Conotruncal cardiac defect, Glioblastoma, Lymphatic metastasis, Ovarian neoplasm

602
Solute carrier family 22 member 11
OAT4, hOAT4
Gout, Iga nephropathy, Major depressive disorder, Obesity, Oligodendroglioma, Systemic lupus erythematosus

603
Solute carrier family 22 member 12
OAT4L, RST, UAT, URAT1, hURAT1
Dalmatian hypouricemia, Gout, Hyperuricemia, Kidney failure, Obesity, Systemic lupus erythematosus

604
Solute carrier family 22 member 15
FLIPT1, PRO34686
Colorectal neoplasm

605
Solute carrier family 22 member 16
CT2, FLIPT2, HEL-S-18, OAT6, OCT6, OKB1, dJ261K5.1
Juvenile arthritis, Bipolar disorder, Colorectal cancer, Juvenile idiopathic arthritis, Major depressive disorder, Melanoma, Oligoarticular juvenile idiopathic arthritis, Psoriasis

606
Solute carrier family 22 member 17
24p3R, BOCT, BOIT, NGALR, NGALR2, NGALR3, hBOIT
Large artery stroke

607
Solute carrier family 22 member 2
Oct-02
Barrett esophagus, Bladder calculus, Cardiovascular disease, Kidney disease, Coronary artery disease, Duodenal ulcer, Esophageal adenocarcinoma, Hyperlipidemia, Hypertensive nephropathy, Kidney failure, Major depressive disorder, Metabolic syndrome, Myocardial infarction, Nephrolithiasis, Obesity
View all (7 more)

608
Solute carrier family 22 member 23
C6orf85
Atrial fibrillation, Attention deficit hyperactivity disorder, Autism, Biliary cirrhosis, Brain injuries, Central nervous system cancer, Color vision deficiency, Colorectal cancer, Crohn disease, Glioblastoma, Glioma, Inflammatory bowel disease, Juvenile idiopathic arthritis, Liver cirrhosis, Ovarian epithelial cancer
View all (7 more)

609
Solute carrier family 22 member 24
NET46
Conotruncal cardiac defect, Kidney failure, Dental caries

610
Solute carrier family 22 member 25
HIMTP, UST6
Conotruncal cardiac defect, Gout