Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
12061 to 12070 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

12061
Solute carrier family 22 member 7
NLT, OAT2, hOAT11
Cardioembolic stroke, Gout, Hearing loss, Hypertension, Stroke, Diabetes mellitus type 2

12062
Solute carrier family 22 member 8
OAT3
Fatty liver, Fatty liver, alcoholic, Liver cirrhosis

12063
Solute carrier family 22 member 9
HOAT4, OAT4, OAT7, UST3H, ust3
Constitutional mismatch repair deficiency syndrome, Lynch syndrome, Constitutional mismatch repair deficiency

12064
Solute carrier family 23 member 1
SLC23A2, SVCT1, YSPL3
Cholelithiasis, Dilated cardiomyopathy, Intracranial hemorrhage

12065
Solute carrier family 23 member 2
NBTL1, SLC23A1, SVCT2, YSPL2
Cholelithiasis, Dementia, Multiple myeloma

12066
Solute carrier family 23 member 3
E2BP3, SVCT3, Yspl1
Schizophrenia

12067
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

12068
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

12069
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)

12070
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