This SuperSeries is composed of the SubSeries listed below.
Overall design: Refer to individual Series
| Accession | PRJNA521172; GEO: GSE126167 |
| Type | Umbrella project |
| Submission | Registration date: 6-Feb-2019
Johns Hopkins School of Medicine |
| Relevance | Superseries |
Project Data:
| Resource Name | Number
of Links |
|---|
| Sequence data |
| SRA Experiments | 16 |
| Other datasets |
| BioSample | 16 |
| GEO DataSets | 4 |
KMT2D loss disrupts cell cycle and hypoxic responses in neurodevelopmental models of Kabuki syndrome encompasses the following 3 sub-projects:
| Project Type | Number of Projects |
| Epigenomics | 1 |
BioProject
accession | Organism | Title |
|---|
| PRJNA521221 | Mus musculus | Chromatin profiling in HT22 hippocampal cells (Johns Hopkins School of Medicine) |
|
| Transcriptome or Gene expression | 2 |
BioProject
accession | Organism | Title |
|---|
| PRJNA521223 | Mus musculus | Genome-wide analysis of gene expression in proliferative dentate gyrus (DG) nuclei of adult wild-type and KMT2D-deficient mice (Johns Hopkins School of Medicine) | | PRJNA521224 | Mus musculus | Genome-wide analysis of gene expression in wild-type and KMT2D-deficient HT22 cells (Johns Hopkins School of Medicine) |
|