Genesⓘ

Dataset:
? Protein-coding genes with reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "S"
621 to 630 of 1631 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

621
Solute carrier family 23 member 3
E2BP3, SVCT3, Yspl1
Schizophrenia

622
Solute carrier family 24 member 1
CSNB1D, HsT17412, NCKX, NCKX1, RODX
Congenital stationary night blindness, Moyamoya angiopathy, Night blindness, congenital stationary, Oguchi disease, Optic atrophy, Retinitis pigmentosa

623
Solute carrier family 24 member 2
NCKX2
Asthma, Atrial fibrillation, Breast cancer, Kidney disease, Color vision deficiency, Dementia, Diabetic neuropathy, Essential tremor, Insomnia, Alzheimer disease, Lung cancer, Mood disorder, Schizophrenia, Scoliosis, Diabetes mellitus, type 2

624
Solute carrier family 24 member 3
NCKX3
Attention deficit hyperactivity disorder, Brain aneurysm, Breast cancer, Adenoid cystic carcinoma, Cataract, Central nervous system cancer, Color vision deficiency, Colorectal cancer, Dementia, Eye disease, Glioblastoma, Glioma, Major depressive disorder, Migraine, Mood disorder
View all (5 more)

625
Solute carrier family 24 member 4
AI2A5, NCKX4, SHEP6, SLC24A2
Alzheimer disease, Amelogenesis imperfecta, Autoimmune thrombocytopenic purpura, Kidney disease, Melanoma, Dementia, Dentin dysplasia, Dentinogenesis imperfecta, Hypomaturation amelogenesis imperfecta, Oligodendroglioma, Skin hair eye pigmentation variation, Venous thromboembolism

626
Solute carrier family 24 member 5
JSX, NCKX5, OCA6, SHEP4
Benign neoplasm of eye, Melanoma, Glaucoma, Oculocutaneous albinism, Open angle glaucoma, Pulmonary arterial hypertension, Scoliosis, Skin cancer, Skin disease, Skin neoplasm, Skin hair eye pigmentation variation

627
Solute carrier family 25 member 1
CIC, CMS23, CTP, D2L2AD, SEA, SLC20A3
Combined d-2- and l-2-hydroxyglutaric aciduria, Presynaptic congenital myasthenic syndromes, Congenital myasthenic syndrome, D-2-hydroxyglutaric aciduria, Mitochondrial disease, Myasthenic syndrome, Presynaptic congenital myasthenic syndrome

628
Solute carrier family 25 member 10
DIC, MTDPS19
Carcinoma, Dental caries, Hearing loss, Mitochondrial complex deficiency, Mitochondrial disease, Mitochondrial dna depletion syndrome

629
Solute carrier family 25 member 11
OGC, PGL6, PPGL6, SLC20A4
Metabolic syndrome, Pheochromocytoma/paraganglioma syndrome, Diabetes mellitus, type 2

630
Solute carrier family 25 member 12
AGC1, ARALAR, DEE39, EIEE39
Rheumatoid arthritis, Asperger syndrome, Autism, Developmental and epileptic encephalopathy, Major depressive disorder, Mitochondrial disease, Schizophrenia, Amyotrophic lateral sclerosis, Diabetes mellitus, type 2