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 1624 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

581
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

582
Solute carrier family 18 member B1
C6orf192, VPAT, dJ55C23.6
Parkinson disease

583
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)

584
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, Thiamine-responsive megaloblastic anemia syndrome
View all (7 more)

585
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

586
Solute carrier family 1 member 1
DCBXA, EAAC1, EAAT3, SCZD18, hEAAC1
Atrophy, Autism, Bipolar disorder, Brain disease, Cognition disorder, Delirium, dementia, and cognitive disorders, Major depressive disorder, Dicarboxylic aminoaciduria, Dicarboxylicaminoaciduria, Endometriosis, Epilepsy, Temporal lobe epilepsy, Cortical development malformation, Ovarian serous carcinoma, Pancreatic cancer
View all (4 more)

587
Solute carrier family 1 member 2
DEE41, EAAT2, EIEE41, GLT-1, GLT1, HBGT
Amyotrophic lateral sclerosis, Eczema, Autoimmune thyroid disease, Bipolar disorder, Breast cancer, Obstructive pulmonary disease, Major depressive disorder, Developmental and epileptic encephalopathy, Diabetes mellitus type 2, Epilepsy, Essential tremor, Hypothyroidism, Mood disorder, Myositis, Schizophrenia
View all (3 more)

588
Solute carrier family 1 member 3
EA6, EAAT1, GLAST, GLAST1
Androgenetic alopecia, Anhedonia, Autism, Bipolar disorder, Epilepsy, Episodic ataxia, Hypertrophic cardiomyopathy, Schizophrenia

589
Solute carrier family 1 member 4
ASCT1, SATT, SPATCCM
Autism, Neurodevelopmental disorder, Macular telangiectasia, Non-specific syndromic intellectual disability

590
Solute carrier family 1 member 5
AAAT, ASCT2, ATBO, M7V1, M7VS1, R16, RDRC
Attention deficit hyperactivity disorder, Gout, Hypotension, Pancreatic neoplasms, Hereditary spastic paraplegia, Substance abuse