Genesⓘ

Dataset:
? Protein-coding genes with reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "S"
611 to 620 of 1631 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

611
Solute carrier family 22 member 3
EMT, EMTH, OCT3
Barrett esophagus, Breast cancer, Cancer, Cardiovascular disease, Colorectal cancer, Coronary artery disease, Diabetes mellitus type 2, Duodenal ulcer, Esophageal adenocarcinoma, Estrogen-receptor negative breast cancer, Hyperlipidemia, Gout, Lung cancer, Metabolic syndrome, Myocardial infarction
View all (10 more)

612
Solute carrier family 22 member 31
-
Breast cancer, Cancer, Central nervous system cancer, Colorectal cancer, Estrogen-receptor negative breast cancer, Glioblastoma, Glioma, Lung cancer, Melanoma, Non-melanoma skin carcinoma, Ovarian cancer, Ovarian serous carcinoma, Prostate cancer, Squamous cell carcinoma

613
Solute carrier family 22 member 4
DFNB60, ETTh, OCTN1
Rheumatoid arthritis, Asthma, Eczema, Breast cancer, Cardiovascular disease, Congenital hearing disorder, Coronary artery disease, Crohn disease, Dermatitis, Hearing loss, Inflammatory bowel disease, Myocardial infarction, Myocarditis, Nasal polyp, Psoriasis
View all (1 more)

614
Solute carrier family 22 member 5
CDSP, OCTN2
Asthma, Eczema, Autism, Autoimmune disease, Cardiomyopathy, Dilated cardiomyopathy, Cardiovascular disease, Carnitine deficiency, Congenital neurologic anomalies, Crohn disease, Dermatitis, Hypertension, Inflammatory bowel disease, Mesothelioma, Myasthenic syndrome
View all (5 more)

615
Solute carrier family 22 member 6
HOAT1, OAT1, PAHT, ROAT1
Calcinosis, Gout, Insomnia

616
Solute carrier family 22 member 7
NLT, OAT2, hOAT11
Cardioembolic stroke, Gout, Hearing loss, Hypertension, Stroke, Diabetes mellitus, type 2

617
Solute carrier family 22 member 8
OAT3
Fatty liver, Fatty liver, alcoholic, Liver cirrhosis

618
Solute carrier family 22 member 9
HOAT4, OAT4, OAT7, UST3H, ust3
Constitutional mismatch repair deficiency syndrome, Lynch syndrome, Constitutional mismatch repair deficiency

619
Solute carrier family 23 member 1
SLC23A2, SVCT1, YSPL3
Cholelithiasis, Dilated cardiomyopathy, Intracranial hemorrhage, Liver cirrhosis

620
Solute carrier family 23 member 2
NBTL1, SLC23A1, SVCT2, YSPL2
Cholelithiasis, Dementia, Multiple myeloma