Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "S"
611 to 620 of 1624 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

611
Solute carrier family 22 member 7
NLT, OAT2, hOAT11
Cardioembolic stroke, Gout, Hearing loss, Hypertension, Stroke, Diabetes mellitus type 2

612
Solute carrier family 22 member 8
OAT3
Fatty liver, Fatty liver, alcoholic, Liver cirrhosis

613
Solute carrier family 22 member 9
HOAT4, OAT4, OAT7, UST3H, ust3
Constitutional mismatch repair deficiency syndrome, Lynch syndrome, Constitutional mismatch repair deficiency

614
Solute carrier family 23 member 1
SLC23A2, SVCT1, YSPL3
Cholelithiasis, Dilated cardiomyopathy, Intracranial hemorrhage

615
Solute carrier family 23 member 2
NBTL1, SLC23A1, SVCT2, YSPL2
Cholelithiasis, Dementia, Multiple myeloma

616
Solute carrier family 23 member 3
E2BP3, SVCT3, Yspl1
Schizophrenia

617
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

618
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

619
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)

620
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