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
12081 to 12090 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

12081
Solute carrier family 17 member 4
KAIA2138
Atherosclerosis, Cardiovascular disease, Gout, Lung cancer, Psoriasis, Schizophrenia, Squamous cell carcinoma

12082
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

12083
Solute carrier family 17 member 6
DNPI, VGLUT2
Bipolar disorder, Learning disorders, Major depressive disorder, Memory disorders, Schizophrenia, Depression

12084
Solute carrier family 17 member 7
BNPI, VGLUT1
Anhedonia, Bipolar disorder, Learning disorders, Memory disorders, Schizophrenia, Seizures

12085
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

12086
Solute carrier family 17 member 9
C20orf59, POROK8, VNUT
Disseminated superficial actinic porokeratosis, Porokeratosis

12087
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

12088
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

12089
Solute carrier family 18 member A3
CMS21, VACHT
Presynaptic congenital myasthenic syndromes, Congenital myasthenic syndrome, Fetal akinesia deformation sequence, Hodgkin lymphoma, Myasthenic syndrome, Pena-shokeir syndrome , Presynaptic congenital myasthenic syndrome

12090
Solute carrier family 18 member B1
C6orf192, VPAT, dJ55C23.6
Parkinson disease