Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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12121 to 12130 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

12121
Solute carrier family 22 member 9
HOAT4, OAT4, OAT7, UST3H, ust3
Constitutional mismatch repair deficiency syndrome, Lynch syndrome, Constitutional mismatch repair deficiency

12122
Solute carrier family 23 member 1
SLC23A2, SVCT1, YSPL3
Cholelithiasis, Dilated cardiomyopathy, Intracranial hemorrhage, Liver cirrhosis

12123
Solute carrier family 23 member 2
NBTL1, SLC23A1, SVCT2, YSPL2
Cholelithiasis, Dementia, Multiple myeloma

12124
Solute carrier family 23 member 3
E2BP3, SVCT3, Yspl1
Schizophrenia

12125
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

12126
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

12127
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)

12128
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

12129
Solute carrier family 24 member 5
JSX, NCKX5, OCA6, SHEP4
Eye neoplasms, Melanoma, Glaucoma, Oculocutaneous albinism, Open angle glaucoma, Pulmonary arterial hypertension, Scoliosis, Skin cancer, Skin disease, Skin neoplasms, Skin hair eye pigmentation variation

12130
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