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"
531 to 540 of 1624 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

531
Solute carrier family 10 member 1
FHCA2, NTCP
Cholelithiasis, Hypercholanemia, Hepatic fibrosis, Hypercholesterolemia, Intrahepatic cholestasis of pregnancy

532
Solute carrier family 10 member 2
ASBT, IBAT, ISBT, NTCP2, PBAM, PBAM1
Bile acid malabsorption, Cholecystolithiasis, Cognition disorder, Diabetes complications, Delirium, dementia, and cognitive disorders, Gallstones, Gout, Intestinal disease, Alzheimer disease, Lung cancer, Major depressive disorder, Nervous system disease, Non-melanoma skin carcinoma, Peripheral arterial disease, Prostate cancer
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533
Solute carrier family 10 member 4
P4
Bipolar disorder, Schizophrenia, Diabetes mellitus type 2

534
Solute carrier family 10 member 6
SOAT
Breast neoplasms, Gout, Metabolic syndrome, Diabetes mellitus type 2

535
Solute carrier family 10 member 7
C4orf13, P7, SSASKS
Anorexia nervosa, Bipolar disorder, Bone fragility with contractures, arterial rupture, and deafness, Cholelithiasis, Obstructive pulmonary disease, Connective tissue disease, Desbuquois syndrome, Headache, Metabolic syndrome, Oligodendroglioma, Osteoporosis-pseudoglioma syndrome, Peptic ulcer disease, Willis-ekbom disease, Diabetes mellitus type 2

536
Solute carrier family 11 member 1
LSH, NRAMP, NRAMP1
Juvenile arthritis, Rheumatoid arthritis, Behcet disease, Buruli ulcer, Ulcerative colitis, Crohn disease, Cystic fibrosis, Atopic dermatitis, Diabetes mellitus type 1, Inflammatory bowel disease, Juvenile idiopathic arthritis, Kidney failure, Systemic lupus erythematosus, Lymphoproliferative syndrome, Multiple sclerosis
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537
Solute carrier family 11 member 2
AHMIO1, DCT1, DMT1, NRAMP2
Amyotrophic lateral sclerosis, Anemia, Hypochromic microcytic anemia, Iron deficiency anemia, Hemochromatosis, Hypochromic anemia, Liver neoplasms, Microcytic anemia, Parkinson disease

538
Solute carrier family 12 member 1
BSC, BSC-1, BSC1, CCC2, NKCC2
Bartter syndrome, Eye neoplasms, Gitelman syndrome, Gout, Nephrolithiasis, Skin cancer, Skin neoplasms, Systemic lupus erythematosus

539
Solute carrier family 12 member 2
BSC, BSC-2, BSC2, CCC1, KILQS, NKCC1, PPP1R141, hNKCC1
Nonsyndromic intellectual disability, Breast cancer, Carcinoid tumor, Carcinoma, Cardiovascular disease, Deafness, Delpire-mcneill syndrome, Epilepsy, Temporal lobe epilepsy, Hearing loss, Hypertension, Intellectual developmental disorder, Lymphatic system disease, Movement disorder, Myopathy
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540
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