PLX066690

GSE134608: RNA-seq analysis of the effects of single and compound deletion of Moz (Kat6a) and/or Dlx5 during mouse craniofacial development

  • Organsim mouse
  • Type RNASEQ
  • Target gene
  • Project ARCHS4

The purpose of these data is to investigate the genetic perturbations which underlie the cleft palate phenotype in Kat6a and Dlx5 mutant mouse embryos. The palate develops from the maxillary portion of the first pharyngeal arches, commencing between E10.5 and E11.5 of mouse gestation. SOURCE: Alexandra Garnham (garnham.a@wehi.edu.au) - Walter and Eliza Hall Institute of Medical Research

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