VIS ID | Virus | Ensembl ID | Gene Type | Target Gene | Oncogene | Tumor Suppressor Gene | NCBI ID | Uniprot ID |
---|---|---|---|---|---|---|---|---|
TVIS10034192 | HBV | ENSG00000168522.13 | protein_coding | FNTA | No | No | 2339 | P49354 |
TVIS30068878 | HIV | ENSG00000168522.13 | protein_coding | FNTA | No | No | 2339 | P49354 |
TVIS20065833 | HPV | ENSG00000168522.13 | protein_coding | FNTA | No | No | 2339 | P49354 |
TVIS44019983 | HTLV-1 | ENSG00000168522.13 | protein_coding | FNTA | No | No | 2339 | P49354 |
Target Gene Table
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TCGA Plot Options
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Drug Information
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Gene | FNTA |
---|---|
DrugBank ID | DB07780 |
Drug Name | Farnesyl diphosphate |
Target ID | BE0002373 |
UniProt ID | P49354 |
Regulation Type | |
PubMed IDs | 10592235 |
Citations | Berman HM, Westbrook J, Feng Z, Gilliland G, Bhat TN, Weissig H, Shindyalov IN, Bourne PE: The Protein Data Bank. Nucleic Acids Res. 2000 Jan 1;28(1):235-42. |
Groups | Experimental |
Direct Classification | Sesquiterpenoids |
SMILES | CC(C)=CCCC(C)=CCCC(C)=CCOP(O)(=O)OP(O)(O)=O |
Pathways | Cerivastatin Action Pathway; Desmosterolosis; Pamidronate Action Pathway; Ibandronate Action Pathway; Simvastatin Action Pathway; Chondrodysplasia Punctata II, X-Linked Dominant (CDPX2); Smith-Lemli-Opitz Syndrome (SLOS); Hyper-IgD Syndrome; Hereditary Coproporphyria (HCP); Porphyria Variegata (PV); Lysosomal Acid Lipase Deficiency (Wolman Disease); Steroid Biosynthesis; Hypercholesterolemia; Acute Intermittent Porphyria; Risedronate Action Pathway; Mevalonic Aciduria; Porphyrin Metabolism; Rosuvastatin Action Pathway; Alendronate Action Pathway; Zoledronate Action Pathway; CHILD Syndrome; Congenital Erythropoietic Porphyria (CEP) or Gunther Disease; Cholesteryl Ester Storage Disease; Lovastatin Action Pathway; Wolman Disease; Fluvastatin Action Pathway; Atorvastatin Action Pathway; Pravastatin Action Pathway |
PharmGKB | |
ChEMBL | CHEMBL69330 |