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 |
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