Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
12111 to 12120 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

12111
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)

12112
Solute carrier family 22 member 24
NET46
Conotruncal cardiac defect, Kidney failure, Dental caries

12113
Solute carrier family 22 member 25
HIMTP, UST6
Conotruncal cardiac defect, Gout

12114
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 (9 more)

12115
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

12116
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)

12117
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)

12118
Solute carrier family 22 member 6
HOAT1, OAT1, PAHT, ROAT1
Calcinosis, Gout, Insomnia

12119
Solute carrier family 22 member 7
NLT, OAT2, hOAT11
Cardioembolic stroke, Gout, Hearing loss, Hypertension, Stroke, Diabetes mellitus type 2

12120
Solute carrier family 22 member 8
OAT3
Fatty liver, Fatty liver, alcoholic, Liver cirrhosis