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Accession: PRJNA471697 ID: 471697

Mechanism sharing between genetic and gestational hypoxia-induced cardiac anomalies (house mouse)

See Genome Information for Mus musculus
Purpose: Mutations in several genetic loci lead to cardiac anomalies, with mutations in transcription factor NKX2-5 gene being one of the largest mutations known. More...
AccessionPRJNA471697; GEO: GSE114532
Data TypeTranscriptome or Gene expression
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
PublicationsMoumne O et al., "Mechanism Sharing Between Genetic and Gestational Hypoxia-Induced Cardiac Anomalies.", Front Cardiovasc Med, 2018;5:100
Grants
  • "Engineering Tissue Mimics to Investigate Congenital Heart Disease" (Grant ID R21 HD090608, National Institute of Child Health & Human Development)
SubmissionRegistration date: 16-May-2018
Physiology and Functional Genomics, University of Florida
RelevanceModel Organism
Project Data:
Resource NameNumber
of Links
Sequence data
SRA Experiments10
Publications
PubMed1
PMC1
Other datasets
BioSample10
GEO DataSets1
GEO Data Details
ParameterValue
Data volume, Supplementary Mbytes5
SRA Data Details
ParameterValue
Data volume, Gbases13
Data volume, Mbytes8063

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