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Accession: PRJNA517446 ID: 517446

Identification of PRDM15 cistrome in the mouse embryo (6.5 d.p.c) (house mouse)

See Genome Information for Mus musculus
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This project is a component of the PRDM15 loss-of-function causes brain malformations through defective embryonic anterior-posterior patterning
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3 additional projects are components of the PRDM15 loss-of-function causes brain malformations through defective embryonic anterior-posterior patterning.
47588 additional projects are related by organism.
Genome-wide binding sites of PRDM15 were identified in 6.5 d.p.c embryos Overall design: ChiP-Seq analysis was performed to identify PRDM15 binding sites in 6.5 d.p.c mouse embryos
AccessionPRJNA517446; GEO: GSE125750
Data TypeEpigenomics
ScopeMultiisolate
OrganismMus musculus[Taxonomy ID: 10090]
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Glires; Rodentia; Myomorpha; Muroidea; Muridae; Murinae; Mus; Mus; Mus musculus
PublicationsMzoughi S et al., "PRDM15 loss of function links NOTCH and WNT/PCP signaling to patterning defects in holoprosencephaly.", Sci Adv, 2020 Jan;6(2):eaax9852
SubmissionRegistration date: 28-Jan-2019
Chromatin, Epigenetics & Differentiation, Institute of Molecular and Cell Biology
RelevanceModel Organism
Project Data:
Resource NameNumber
of Links
Sequence data
SRA Experiments2
Publications
PubMed1
PMC1
Other datasets
BioSample2
GEO DataSets1
GEO Data Details
ParameterValue
Data volume, Supplementary Mbytes493
SRA Data Details
ParameterValue
Data volume, Gbases6
Data volume, Mbytes2670

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