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
12251 to 12260 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

12251
Solute carrier family 5 member 2
SGLT2
Renal glycosuria

12252
Solute carrier family 5 member 3
BCW2, SMIT, SMIT1, SMIT2
Bipolar disorder, Renal cell carcinoma, Ischemic heart disease, Coronary artery disease, Bipolar depression, Myocardial ischemia

12253
Solute carrier family 5 member 5
NIS, TDH1
Breast neoplasms, Hepatocellular carcinoma, Cholangiocarcinoma, Congenital hypothyroidism, Thyroid dyshormonogenesis, Glioma, Kidney neoplasms, Melanoma, Ovarian neoplasms, Prostatic neoplasms, Thyroid neoplasms

12254
Solute carrier family 5 member 6
COMNB, NERIB, SMVT, SMVTD, hSMVT
Genetic neurodegenerative disease, Metabolic syndrome, Neurodevelopmental disorder, Diabetes mellitus type 2, Uterine fibroid

12255
Solute carrier family 5 member 7
CHT, CHT1, CMS20, DHMNVP, HMN7A, HMND7, hCHT1
Charcot-marie-tooth disease, Presynaptic congenital myasthenic syndromes, Congenital myasthenic syndrome, Distal hereditary motor neuropathy, Distal spinal muscular atrophy, Hereditary motor and sensory neuropathies, Major depressive disorder, Mood disorder, Myasthenic syndrome, Presynaptic congenital myasthenic syndrome, Depression, Schizophrenia

12256
Solute carrier family 5 member 8
AIT, SMCT, SMCT1
Colonic neoplasms, Colorectal cancer, Hyperuricemia

12257
Solute carrier family 5 member 9
SGLT4
Gout

12258
Solute carrier family 66 member 1
LAAT-1, LAAT1, PQLC2
Hypothyroidism, Nephropathic cystinosis

12259
Solute carrier family 66 member 2
PQLC1
Dementia, Schizophrenia, Diabetes mellitus type 2

12260
Solute carrier family 66 member 3
C2orf22, PQLC3
Liver neoplasms, Hypertension, Uterine fibroid