Ventricular Septal Defect

About the Disease
Ventricular Septal Defect, also known as ventricular septal defects, is related to tetralogy of fallot and heart septal defect. An important gene associated with Ventricular Septal Defect is FOXP4 (Forkhead Box P4), and among its related pathways/superpathways are Human Embryonic Stem Cell Pluripotency and Mesenchymal Stem Cells and Lineage-specific Markers. The drugs Salbutamol and Adrenergic Agonists have been mentioned in the context of this disorder. Affiliated tissues include heart, lung and smooth muscle, and related phenotypes are Increased shRNA abundance (Z-score > 2) and Increased shRNA abundance (Z-score > 2)

Common Targets
POLR1HASP | GATA4 | NFATC1 | GDF1 | TNFSF11 | FGFR1 | MTRR | PLAGL1 | TCF21 | KDR | NKX2-5 | HAS2 | DSP | HOXA1 | G7422 | JUP | NRP1 | GATA5 | GPC5 | NR2F2 | FIGN | STX18-AS1 | SMAD3 | NKX2-6 | MTR | ABL1 | BCL6 | TWIST1 | HEY2 | SCO2 | FMN1 | BAG3 | POLR1H | HOMEZ | SCN10A

Note: If you'd like to get a target analysis report for Ventricular Septal Defect, or if you are interested to learn how our AI-powered BDE-Chem can design therapeutic molecules to interact with the target(s) above against the disease of Ventricular Septal Defect at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.tech.

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