Target Gene Table
VIS IDVirusEnsembl IDGene TypeTarget GeneOncogeneTumor Suppressor GeneNCBI IDUniprot ID
TVIS10014061HBVENSG00000079215.15protein_codingSLC1A3NoNo6507A0A087WT87
A0A087X0U3
P43003
Q7Z5T0
Q8N169
TVIS10044297HBVENSG00000079215.15protein_codingSLC1A3NoNo6507A0A087WT87
A0A087X0U3
P43003
Q7Z5T0
Q8N169
TVIS10044298HBVENSG00000079215.15protein_codingSLC1A3NoNo6507A0A087WT87
A0A087X0U3
P43003
Q7Z5T0
Q8N169
TVIS20010139HPVENSG00000079215.15protein_codingSLC1A3NoNo6507A0A087WT87
A0A087X0U3
P43003
Q7Z5T0
Q8N169
TVIS20034512HPVENSG00000079215.15protein_codingSLC1A3NoNo6507A0A087WT87
A0A087X0U3
P43003
Q7Z5T0
Q8N169
TVIS20045277HPVENSG00000079215.15protein_codingSLC1A3NoNo6507A0A087WT87
A0A087X0U3
P43003
Q7Z5T0
Q8N169
TCGA Plot Options
Drug Information
GeneSLC1A3
DrugBank IDDB00142
Drug NameGlutamic acid
Target IDBE0001115
UniProt IDP43003
Regulation Type
PubMed IDs16855093; 17088867; 16959378
CitationsGlowatzki E, Cheng N, Hiel H, Yi E, Tanaka K, Ellis-Davies GC, Rothstein JD, Bergles DE: The glutamate-aspartate transporter GLAST mediates glutamate uptake at inner hair cell afferent synapses in the mammalian cochlea. J Neurosci. 2006 Jul 19;26(29):7659-64.@@Beart PM, O'Shea RD: Transporters for L-glutamate: an update on their molecular pharmacology and pathological involvement. Br J Pharmacol. 2007 Jan;150(1):5-17. Epub 2006 Nov 6.@@Nickell J, Salvatore MF, Pomerleau F, Apparsundaram S, Gerhardt GA: Reduced plasma membrane surface expression of GLAST mediates decreased glutamate regulation in the aged striatum. Neurobiol Aging. 2007 Nov;28(11):1737-48. Epub 2006 Sep 7.
GroupsApproved; Nutraceutical
Direct ClassificationGlutamic acid and derivatives
SMILESN[C@@H](CCC(O)=O)C(O)=O
PathwaysHistidinemia; Guanidinoacetate Methyltransferase Deficiency (GAMT Deficiency); 3-Methylglutaconic Aciduria Type I; beta-Ketothiolase Deficiency; Purine Nucleoside Phosphorylase Deficiency; Tyrosine Metabolism; Ketoprofen Action Pathway; Glutamate Metabolism; Argininosuccinic Aciduria; Salla Disease/Infantile Sialic Acid Storage Disease; Tyrosinemia Type I; Hyperinsulinism-Hyperammonemia Syndrome; 2-Methyl-3-hydroxybutryl-CoA Dehydrogenase Deficiency; Glutaric Aciduria Type I; Propanoate Metabolism; Celecoxib Action Pathway; Glycine and Serine Metabolism; Suprofen Action Pathway; Indomethacin Action Pathway; Carbamoyl Phosphate Synthetase Deficiency; Sialuria or French Type Sialuria; Ibuprofen Action Pathway; Saccharopinuria/Hyperlysinemia II; Histidine Metabolism; Arginine and Proline Metabolism; Purine Metabolism; Diflunisal Action Pathway; Etodolac Action Pathway; Ammonia Recycling
PharmGKBPA449776
ChEMBLCHEMBL575060