VIS ID | Virus | Ensembl ID | Gene Type | Target Gene | Oncogene | Tumor Suppressor Gene | NCBI ID | Uniprot ID |
---|---|---|---|---|---|---|---|---|
TVIS42000526 | EBV | ENSG00000074410.14 | protein_coding | CA12 | No | No | 771 | B3KUB4 O43570 |
TVIS10040395 | HBV | ENSG00000074410.14 | protein_coding | CA12 | No | No | 771 | B3KUB4 O43570 |
TVIS10040396 | HBV | ENSG00000074410.14 | protein_coding | CA12 | No | No | 771 | B3KUB4 O43570 |
TVIS44011028 | HTLV-1 | ENSG00000074410.14 | protein_coding | CA12 | No | No | 771 | B3KUB4 O43570 |
Target Gene Table
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TCGA Plot Options
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Drug Information
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Gene | CA12 |
---|---|
DrugBank ID | DB00774 |
Drug Name | Hydroflumethiazide |
Target ID | BE0001653 |
UniProt ID | O43570 |
Regulation Type | inhibitor |
PubMed IDs | 19119014 |
Citations | Temperini C, Cecchi A, Scozzafava A, Supuran CT: Carbonic anhydrase inhibitors. Comparison of chlorthalidone, indapamide, trichloromethiazide, and furosemide X-ray crystal structures in adducts with isozyme II, when several water molecules make the difference. Bioorg Med Chem. 2009 Feb 1;17(3):1214-21. doi: 10.1016/j.bmc.2008.12.023. Epub 2008 Dec 24. |
Groups | Approved; Investigational; Withdrawn |
Direct Classification | 1,2,4-benzothiadiazine-1,1-dioxides |
SMILES | NS(=O)(=O)C1=CC2=C(NCNS2(=O)=O)C=C1C(F)(F)F |
Pathways | Hydroflumethiazide Action Pathway |
PharmGKB | PA164752557 |
ChEMBL | CHEMBL1763 |