Target Gene Table
VIS IDVirusEnsembl IDGene TypeTarget GeneOncogeneTumor Suppressor GeneNCBI IDUniprot ID
TVIS10017865HBVENSG00000166224.19protein_codingSGPL1NoNo8879O95470
TVIS10050166HBVENSG00000166224.19protein_codingSGPL1NoNo8879O95470
TVIS30000162HIVENSG00000166224.19protein_codingSGPL1NoNo8879O95470
TVIS30005619HIVENSG00000166224.19protein_codingSGPL1NoNo8879O95470
TVIS30005620HIVENSG00000166224.19protein_codingSGPL1NoNo8879O95470
TVIS30027790HIVENSG00000166224.19protein_codingSGPL1NoNo8879O95470
TVIS30027791HIVENSG00000166224.19protein_codingSGPL1NoNo8879O95470
TVIS30027792HIVENSG00000166224.19protein_codingSGPL1NoNo8879O95470
TVIS30027793HIVENSG00000166224.19protein_codingSGPL1NoNo8879O95470
TVIS30027794HIVENSG00000166224.19protein_codingSGPL1NoNo8879O95470
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Drug Information
GeneSGPL1
DrugBank IDDB00114
Drug NamePyridoxal phosphate
Target IDBE0000778
UniProt IDO95470
Regulation Typecofactor
PubMed IDs15522238; 11377878
CitationsIkeda M, Kihara A, Igarashi Y: Sphingosine-1-phosphate lyase SPL is an endoplasmic reticulum-resident, integral membrane protein with the pyridoxal 5'-phosphate binding domain exposed to the cytosol. Biochem Biophys Res Commun. 2004 Dec 3;325(1):338-43.@@Bobbin RP: PPADS, an ATP antagonist, attenuates the effects of a moderately intense sound on cochlear mechanics. Hear Res. 2001 Jun;156(1-2):10-6.
GroupsApproved; Investigational; Nutraceutical
Direct ClassificationPyridoxals and derivatives
SMILESCC1=NC=C(COP(O)(O)=O)C(C=O)=C1O
PathwaysHistidinemia; 3-Methylglutaconic Aciduria Type I; Guanidinoacetate Methyltransferase Deficiency (GAMT Deficiency); beta-Ketothiolase Deficiency; Tyrosine Metabolism; Disulfiram Action Pathway; Hyperprolinemia Type II; Glutamate Metabolism; Argininosuccinic Aciduria; Tyrosinemia Type I; Hyperinsulinism-Hyperammonemia Syndrome; Porphyrin Metabolism; 2-Methyl-3-hydroxybutryl-CoA Dehydrogenase Deficiency; Glutaric Aciduria Type I; Propanoate Metabolism; Taurine and Hypotaurine Metabolism; Catecholamine Biosynthesis; Glycine and Serine Metabolism; Carnitine Synthesis; Tyrosinemia Type 3 (TYRO3); Selenoamino Acid Metabolism; Carbamoyl Phosphate Synthetase Deficiency; Hyperprolinemia Type I; Saccharopinuria/Hyperlysinemia II; Histidine Metabolism; Cystathionine beta-Synthase Deficiency; Arginine and Proline Metabolism; Starch and Sucrose Metabolism; Globoid Cell Leukodystrophy; Ammonia Recycling
PharmGKBPA164749650
ChEMBLCHEMBL82202