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
Showing genes starting with "S"
801 to 810 of 1624 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

801
Solute carrier family 5 member 2
SGLT2
Renal glycosuria

802
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

803
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

804
Solute carrier family 5 member 6
COMNB, NERIB, SMVT, SMVTD, hSMVT
Genetic neurodegenerative disease, Metabolic syndrome, Neurodevelopmental disorder, Diabetes mellitus type 2, Uterine fibroid

805
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

806
Solute carrier family 5 member 8
AIT, SMCT, SMCT1
Colonic neoplasms, Colorectal cancer, Hyperuricemia

807
Solute carrier family 5 member 9
SGLT4
Gout

808
Solute carrier family 66 member 1
LAAT-1, LAAT1, PQLC2
Hypothyroidism, Nephropathic cystinosis

809
Solute carrier family 66 member 2
PQLC1
Dementia, Schizophrenia, Diabetes mellitus type 2

810
Solute carrier family 66 member 3
C2orf22, PQLC3
Liver neoplasms, Hypertension, Uterine fibroid