Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "S"
801 to 810 of 1203 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

801
Solute carrier family 12 member 3
NCC, NCCT, TSC
Bartter syndrome, Breast cancer, Hypertension, Hypokalemia-hypomagnesemia, Genetic renal tubular disease, Gitelman syndrome, Kidney disease, Lymphoid leukemia, Metabolic syndrome, Nephrolithiasis, Diabetes mellitus, type 2, Vascular disease

802
Solute carrier family 12 member 4
CTC-479C5.17, KCC1, hKCC1
Bipolar disorder

803
Solute carrier family 14 member 1 (Kidd blood group)
HUT11, HUT11A, HsT1341, JK, Jk(a), Jk(b), RACH1, RACH2, UT-B1, UT1, UTE
Hemolytic anemia, Autoimmune hemolytic anemia, Urinary bladder cancer

804
Solute carrier family 15 member 2
PEPT2
Asthma, Autoimmune disease, Melanoma, Multiple sclerosis

805
Solute carrier family 16 member 1
HHF7, MCT, MCT1, MCT1D
Autism, Colonic neoplasm, Hyperinsulinemic hypoglycemia, Hyperinsulinism, Osteoarthritis

806
Solute carrier family 16 member 2
AHDS, DXS128, DXS128E, MCT 7, MCT 8, MCT7, MCT8, MRX22, XPCT
Allan-herndon-dudley syndrome, Autism, Cholelithiasis, Hypothyroidism, Intellectual developmental disorder, Spastic paraplegia, Hereditary spastic paraplegia

807
Solute carrier family 17 member 1
NAPI-1, NPT-1, NPT1
Alzheimer disease, Celiac disease, Dental caries, Gout, Insomnia, Irritable bowel syndrome, Liver cirrhosis, Major depressive disorder, Metabolic syndrome, Psoriasis, Systemic lupus erythematosus, Diabetes mellitus, type 2

808
Solute carrier family 34 member 1
FRTS2, HCINF2, NAPI-3, NPHLOP1, NPT2, NPTIIa, SLC11, SLC17A2
Asthma, Bladder calculus, Bone disease, Stone disease, Kidney disease, Crohn disease, De toni-debre-fanconi syndrome, Hypercalcemia, Infantile hypercalcemia, Hypercalciuria, Hypophosphatemic rickets, Inflammatory bowel disease, Kidney failure, Nephrolithiasis, Osteogenesis imperfecta
View all (3 more)

809
Solute carrier family 18 member A1
CGAT, VAT1, VMAT1
Amyotrophic lateral sclerosis, Bipolar disorder, Bipolar depression, Major depressive disorder, Depression, Metabolic syndrome, Schizophrenia, Diabetes mellitus, type 2

810
Solute carrier family 18 member A2
PKDYS2, SVAT, SVMT, VAT2, VMAT2
Bipolar disorder, Brain edema, Major depressive disorder, Depression, Nervous system disease, Parkinson disease, Secondary parkinson disease, Parkinsonism-dystonia, Schizophrenia