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"
581 to 590 of 1631 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

581
Solute carrier family 17 member 7
BNPI, VGLUT1
Anhedonia, Bipolar disorder, Learning disorders, Memory disorders, Schizophrenia, Seizures

582
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

583
Solute carrier family 17 member 9
C20orf59, POROK8, VNUT
Disseminated superficial actinic porokeratosis, Porokeratosis

584
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

585
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

586
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

587
Solute carrier family 18 member B1
C6orf192, VPAT, dJ55C23.6
Parkinson disease

588
Solute carrier family 19 member 1
CHMD, FOLT, IFC-1, IFC1, IMD114, MEGAF, REFC, RFC, RFC1, RFT-1, hRFC, hSLC19A1
Autism, Cataract, Cleft lip, Cleft palate, Colonic neoplasms, Colorectal neoplasms, Combined immunodeficiency disease, Complete unilateral cleft lip, Discordant ventriculoarterial connection, Down syndrome, Glaucoma, Immunodeficiency, Knobloch syndrome, Macular dystrophy, Megaloblastic anemia
View all (6 more)

589
Solute carrier family 19 member 2
TC1, THMD1, THT1, THTR1, TRMA
Megaloblastic anemia, Angioedema, Atrial fibrillation, Blood coagulation disorder, Cardiovascular disease, Venous hypertension, Venous insufficiency, Congenital ear anomaly, Cor pulmonale, Diabetes mellitus, Edema, Endometriosis, Heart disease, Lipoma, Liver cirrhosis
View all (7 more)

590
Solute carrier family 19 member 3
BBGD, THMD2, THTR2, hTHTR2, thTr-2
Basal ganglia disease, Biotin-responsive basal ganglia disease, Biotin-thiamine-responsive basal ganglia disease, Central nervous system cancer, Glioblastoma, Glioma, Leigh syndrome, Nephrotic syndrome, Neurotic disorder, Obesity, Spastic paraplegia, Thiamine-responsive encephalopathy