Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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11981 to 11990 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

11981
Solute carrier family 10 member 1
FHCA2, NTCP
Cholelithiasis, Hypercholanemia, Hepatic fibrosis, Hypercholesterolemia, Intrahepatic cholestasis of pregnancy

11982
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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11983
Solute carrier family 10 member 4
P4
Bipolar disorder, Schizophrenia, Diabetes mellitus type 2

11984
Solute carrier family 10 member 6
SOAT
Breast neoplasms, Gout, Metabolic syndrome, Diabetes mellitus type 2

11985
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

11986
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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11987
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

11988
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

11989
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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11990
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