Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "S"
801 to 810 of 1631 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

801
Solute carrier family 52 member 2
BVVLS2, D15Ertd747e, GPCR41, GPR172A, HuPAR-1, PAR1, RFT3, RFVT2, hRFT3
Auditory neuropathy, Brown-vialetto-van laere syndrome, Riboflavin transporter deficiency, Hearing loss

802
Solute carrier family 52 member 3
BVVLS, BVVLS1, C20orf54, RFT2, RFVT3, bA371L19.1, hRFT2
Alzheimer disease, Auditory neuropathy, Brown-vialetto-van laere syndrome, Bulbar palsy, Esophageal squamous cell carcinoma, Obstructive sleep apnea syndrome, Oligodendroglioma, Prostate cancer, Riboflavin transporter deficiency

803
Solute carrier family 5 member 1
D22S675, NAGT, SGLT-1, SGLT1
Congenital glucose-galactose malabsorption, Renal glycosuria, Gout

804
Solute carrier family 5 member 11
KST1, RKST1, SGLT6, SMIT2
Atrial fibrillation, Gout, Lupus nephritis

805
Solute carrier family 5 member 12
SMCT2
Asthma, Dental caries, Erectile dysfunction

806
Solute carrier family 5 member 2
SGLT2
Renal glycosuria

807
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

808
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

809
Solute carrier family 5 member 6
COMNB, NERIB, SMVT, SMVTD, hSMVT
Genetic neurodegenerative disease, Metabolic syndrome, Neurodevelopmental disorder, Diabetes mellitus type 2, Uterine fibroid

810
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