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
12091 to 12100 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

12091
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)

12092
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)

12093
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

12094
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, Leprosy, Cortical development malformation, Ovarian serous carcinoma
View all (5 more)

12095
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)

12096
Solute carrier family 1 member 3
EA6, EAAT1, GLAST, GLAST1
Androgenetic alopecia, Anhedonia, Autism, Bipolar disorder, Epilepsy, Episodic ataxia, Hypertrophic cardiomyopathy, Schizophrenia

12097
Solute carrier family 1 member 4
ASCT1, SATT, SPATCCM
Autism, Neurodevelopmental disorder, Macular telangiectasia, Non-specific syndromic intellectual disability

12098
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

12099
Solute carrier family 1 member 6
EAAT4
Bipolar disorder, Major depressive disorder, Schizophrenia, Squamous cell carcinoma, Depression

12100
Solute carrier family 1 member 7
AAAT, EAAT5
Dementia, Systemic lupus erythematosus