Genes | GeDiPNet - Gene Disease Pathway & Associations

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12041 to 12050 of 15448 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
12041	201780	SLC10A4	Solute carrier family 10 member 4	P4	Bipolar disorder, Schizophrenia, Diabetes mellitus type 2
12042	345274	SLC10A6	Solute carrier family 10 member 6	SOAT	Breast neoplasms, Gout, Metabolic syndrome, Diabetes mellitus type 2
12043	84068	SLC10A7	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
12044	6556	SLC11A1	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, Leishmaniasis, Leprosy, Systemic lupus erythematosus View all (6 more)
12045	4891	SLC11A2	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
12046	6557	SLC12A1	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
12047	6558	SLC12A2	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 View all (6 more)
12048	6559	SLC12A3	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
12049	6560	SLC12A4	Solute carrier family 12 member 4	CTC-479C5.17, KCC1, hKCC1	Bipolar disorder
12050	57468	SLC12A5	Solute carrier family 12 member 5	DEE34, EIEE34, EIG14, KCC2, hKCC2	Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Developmental and epileptic encephalopathy, Epilepsy, Epilepsy of infancy with migrating focal seizures, Idiopathic generalized epilepsy, Temporal lobe epilepsy, Hyperalgesia, Major depressive disorder, Malignant migrating partial seizures of infancy, Mood disorder, Movement disorder, Neurotic disorder, Psychiatric disorders View all (4 more)

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