Pathway panels
Browse qRT-PCR primers grouped by biological pathway, from Reactome.
1862 panels
- Signaling by Type 1 Insulin-like Growth Factor 1 Receptor (IGF1R) 4 genes
- Synthesis of IPs in the nucleus 4 genes
- Synthesis of PIPs in the nucleus 4 genes
- TET1,2,3 and TDG demethylate DNA 4 genes
- TFAP2 (AP-2) family regulates transcription of other transcription factors 4 genes
- TGFBR1 LBD Mutants in Cancer 4 genes
- TGFBR3 regulates activin signaling 4 genes
- Toll Like Receptor TLR6:TLR2 Cascade 4 genes
- Toxicity of botulinum toxin type A (botA) 4 genes
- Transcriptional activation of cell cycle inhibitor p21 4 genes
- Utilization of Ketone Bodies 4 genes
- Wax biosynthesis 4 genes
- rRNA processing in the mitochondrion 4 genes
- 5-Phosphoribose 1-diphosphate biosynthesis 3 genes
- ABO blood group biosynthesis 3 genes
- ARL13B-mediated ciliary trafficking of INPP5E 3 genes
- Activated NTRK3 signals through PLCG1 3 genes
- Activation of BIM and translocation to mitochondria 3 genes
- Activation of BMF and translocation to mitochondria 3 genes
- Adrenaline signalling through Alpha-2 adrenergic receptor 3 genes
- Autointegration results in viral DNA circles 3 genes
- Beta oxidation of myristoyl-CoA to lauroyl-CoA 3 genes
- Beta oxidation of palmitoyl-CoA to myristoyl-CoA 3 genes
- Biosynthesis of DHA-derived SPMs 3 genes
- Biosynthesis of aspirin-triggered D-series resolvins 3 genes
- Breakdown of the nuclear lamina 3 genes
- CaM pathway 3 genes
- Cellular response to hypoxia 3 genes
- Ceramide signalling 3 genes
- Defective AMN causes MGA1 3 genes
- Defective AVP does not bind AVPR1A,B and causes neurohypophyseal diabetes insipidus (NDI) 3 genes
- Defective CUBN causes MGA1 3 genes
- Defective DPM1 causes DPM1-CDG 3 genes
- Defective DPM2 causes DPM2-CDG 3 genes
- Defective DPM3 causes DPM3-CDG 3 genes
- Defective F8 cleavage by thrombin 3 genes
- Defective F8 sulfation at Y1699 3 genes
- Defective F9 variant does not activate FX 3 genes
- Defective Mismatch Repair Associated With MSH2 3 genes
- Defective NEU1 causes sialidosis 3 genes
Pathway data from Reactome, released under CC0.