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
12021 to 12030 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

12021
Solute carrier family 17 member 2
NPT3
Liver cirrhosis, Dental caries, Gout, Iron metabolism disorder, Large artery stroke, Metabolic syndrome, Nonalcoholic fatty liver disease, Peripheral arterial disease, Polycythemia vera, Psoriasis, Systemic lupus erythematosus

12022
Solute carrier family 17 member 3
GOUT4, NPT4, UAQTL4
Gouty arthritis, Breast cancer, Color vision deficiency, Estrogen-receptor negative breast cancer, Gout, Major depressive disorder, Nephrolithiasis, Osteoarthritis, Rheumatoid arthritis, Schizophrenia, Systemic lupus erythematosus, Diabetes mellitus type 1, Hyperuricemia

12023
Solute carrier family 17 member 4
KAIA2138
Atherosclerosis, Cardiovascular disease, Gout, Lung cancer, Psoriasis, Schizophrenia, Squamous cell carcinoma

12024
Solute carrier family 17 member 5
AST, ISSD, NSD, SD, SIALIN, SIASD, SLD, VEAT
Color vision deficiency, Desbuquois syndrome, Focal glomerulosclerosis, Gitelman syndrome, Salla disease, Intracerebral hemorrhage, Melanoma

12025
Solute carrier family 17 member 6
DNPI, VGLUT2
Bipolar disorder, Learning disorders, Major depressive disorder, Memory disorders, Schizophrenia, Depression

12026
Solute carrier family 17 member 7
BNPI, VGLUT1
Anhedonia, Bipolar disorder, Learning disorders, Memory disorders, Schizophrenia, Seizures

12027
Solute carrier family 17 member 8
DFNA25, VGLUT3
Auditory neuropathy, Isolated sensorineural deafness, Nonsyndromic hearing loss, Deafness, Hereditary hearing loss, Non-small cell lung carcinoma, Squamous cell carcinoma

12028
Solute carrier family 17 member 9
C20orf59, POROK8, VNUT
Disseminated superficial actinic porokeratosis, Porokeratosis

12029
Solute carrier family 18 member A1
CGAT, VAT1, VMAT1
Amyotrophic lateral sclerosis, Bipolar disorder, Bipolar depression, Major depressive disorder, Metabolic syndrome, Schizophrenia, Diabetes mellitus type 2

12030
Solute carrier family 18 member A2
PKDYS2, SVAT, SVMT, VAT2, VMAT2
Bipolar disorder, Brain edema, Major depressive disorder, Nervous system disease, Parkinson disease, Secondary parkinson disease, Parkinsonism-dystonia, Schizophrenia, Depression