See
Genome Information for Mus musculus
Navigate Up
Navigate Across
2 additional projects are components of the KMT2D loss disrupts cell cycle and hypoxic responses in neurodevelopmental models of Kabuki syndrome.
We conducted genome wide transcription profiling by RNA-seq in a mouse hippocampal cell line (HT22), comparing cells with CRISPR-Cas9 mediated deletion of the KMT2D enzymatic SET methyltransferase domain to the parental cell line
Overall design: RNA-seq in wild-type and KMT2D-deficient (SET domain deletion) HT22 cells
| Accession | PRJNA521224; GEO: GSE126165 |
| Data Type | Transcriptome or Gene expression |
| Scope | Multiisolate |
| Organism | Mus musculus[Taxonomy ID: 10090] Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Glires; Rodentia; Myomorpha; Muroidea; Muridae; Murinae; Mus; Mus; Mus musculus |
| Submission | Registration date: 6-Feb-2019
Johns Hopkins School of Medicine |
| Relevance | Model Organism |
Project Data:
| Resource Name | Number
of Links |
|---|
| Sequence data |
| SRA Experiments | 12 |
| Other datasets |
| BioSample | 12 |
| GEO DataSets | 1 |