| Enhancer ID: | E_02_0737 |
| Species: | human |
| Position : | chr15:99562591-99564591 |
| Biosample name: | |
| Experiment class : | High+Lowthroughput |
| Enhancer type: | Enhancer |
| Disease: | Mitochondrial disorder |
| Pubmed ID: | 32209973 |
| Enhancer experiment: | Transfection, Western blot, immunofluorescence, cell viability assays |
| Enhancer experiment description: | we identify the transcription factor myocyte enhancer factor 2A (MEF2A) as the common link between OT and cellular changes symptomatic for ASD, encompassing neuronal morphology, connectivity, and mitochondrial function |
| Target gene : | MEF2A |
| Strong evidence: | qRT-PCR,qPCR,ChIP,3C |
| Less strong evidence: | RNA-Seq |
| Target gene experiment description: | we identify the transcription factor myocyte enhancer factor 2A (MEF2A) as the common link between OT and cellular changes symptomatic for ASD, encompassing neuronal morphology, connectivity, and mitochondrial function |
| TF name : | -- |
| TF experiment: | ???Western blot???????????? |
| TF experiment description: | we identify the transcription factor myocyte enhancer factor 2A (MEF2A) as the common link between OT and cellular changes symptomatic for ASD, encompassing neuronal morphology, connectivity, and mitochondrial function |
| Enhancer function : | we identify the transcription factor myocyte enhancer factor 2A (MEF2A) as the common link between OT and cellular changes symptomatic for ASD, encompassing neuronal morphology, connectivity, and mitochondrial function |
| Enhancer function experiment: | Immunohistochemical staining |
| Enhancer function experiment description: |
we identify the transcription factor myocyte enhancer factor 2A (MEF2A) as the common link between OT and cellular changes symptomatic for ASD, encompassing neuronal morphology, connectivity, and mitochondrial function |
| SNP ID: | -- |
| GeneName | Pathway Name | Source | Gene Number |
|---|