Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "S"

791 to 800 of 1203 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
791	6542	SLC7A2	Solute carrier family 7 member 2	ATRC2, CAT-2A, CAT-2B, CAT2, HCAT2, SLC7A2A, SLC7A2B	Alzheimer disease, Basal cell carcinoma, Cerebral amyloid angiopathy, Dementia, Orofacial cleft
792	6546	SLC8A1	Solute carrier family 8 member A1	NCX1	Autoimmune neurological syndrome, Asthma, Bone fracture, Clonal hematopoiesis, Color vision deficiency, Duchenne muscular dystrophy, Hypertension, Myocardial ischemia, Obesity, Periapical periodontitis, Schizophrenia, Seizures, Status epilepticus, Diabetes mellitus, type 2
793	6547	SLC8A3	Solute carrier family 8 member A3	NCX3	Autism, Bipolar disorder, Cystic fibrosis, Dementia, Peripheral arterial disease, Schizophrenia, Scoliosis, Seizures, Status epilepticus, Tuberculosis
794	6548	SLC9A1	Solute carrier family 9 member A1	APNH, LIKNS, NHE-1, NHE1, PPP1R143	Barrett esophagus, Cardiomyopathy, Cerebellar dysfunction with variable cognitive and behavioral abnormalities, Experimental diabetes, Edema, Heart failure, Hypertrophic cardiomyopathy, Cerebellar ataxia with hearing loss
795	6549	SLC9A2	Solute carrier family 9 member A2	NHE2	Asthma, Eczema, Crohn disease, Edema, Endometriosis, Leprosy, Respiratory system disease
796	6550	SLC9A3	Solute carrier family 9 member A3	DIAR8, NHE-3, NHE3	Autism, Cystic fibrosis, Experimental diabetes, Diarrhea, Diverticular disease, Dysentery, Edema, Hypotension, Intestinal obstruction, Lung disease, Schizophrenia
797	6555	SLC10A2	Solute carrier family 10 member 2	ASBT, IBAT, ISBT, NTCP2, PBAM, PBAM1	Bile acid malabsorption, Cholecystolithiasis, Cognition disorder, Complications of diabetes mellitus, Delirium, dementia, and cognitive disorders, Diabetes complications, Gallstones, Gout, Intestinal disease, Alzheimer disease, Lung cancer, Major depressive disorder, Nervous system disease, Non-melanoma skin carcinoma, Peripheral arterial disease View all (2 more)
798	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, Human immunodeficiency virus infection, Inflammatory bowel disease, Juvenile idiopathic arthritis, Kidney failure, Leishmaniasis, Leprosy View all (9 more)
799	6557	SLC12A1	Solute carrier family 12 member 1	BSC, BSC-1, BSC1, CCC2, NKCC2	Bartter syndrome, Gitelman syndrome, Gout, Nephrolithiasis, Skin cancer, Skin neoplasm, Systemic lupus erythematosus
800	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)

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