Homo sapiens (ID 339028) - BioProject

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Accession: PRJNA339028 ID: 339028

Homo sapiens (human)

See Genome Information for Homo sapiens

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2 additional projects are components of the Disease Model of GATA4 Mutation Reveals Transcription Factor Cooperativity in Human Cardiogenesis.

Heterozygous mutations in GATA4 cause congenital heart defects and cardiomyopathy through unknown mechanisms. More...

Accession	PRJNA339028; GEO: GSE85628
Data Type	Epigenomics
Scope	Multiisolate
Organism	Homo sapiens[Taxonomy ID: 9606] Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
Publications	Ang YS et al., "Disease Model of GATA4 Mutation Reveals Transcription Factor Cooperativity in Human Cardiogenesis.", Cell, 2016 Dec 15;167(7):1734-1749.e22
Submission	Registration date: 15-Aug-2016 Gladstone Institute, UCSF
Relevance	Medical

Project Data:

Parameter	Value
Data volume, Supplementary Mbytes	53

Parameter	Value
Data volume, Gbases	111
Data volume, Mbytes	35211

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