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Accession: PRJNA291288 ID: 291288

Mus musculus breed:C57BL/6J (house mouse)

Mus musculus breed:C57BL/6J Raw sequence reads

See Genome Information for Mus musculus
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47588 additional projects are related by organism.
In principle, dominant mutations in the rhodopsin gene—the major cause of autosomal dominant retinitis pigmentosa—could be edited in patients by homologous recombination (HR) or nonhomologous end joining (NHEJ) of targeted genomic breaks. More...
AccessionPRJNA291288
Data TypeRaw sequence reads
ScopeMonoisolate
OrganismMus musculus[Taxonomy ID: 10090]
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Glires; Rodentia; Myomorpha; Muroidea; Muridae; Murinae; Mus; Mus; Mus musculus
Grants
  • "Robert A Welch Foundation Chair in Chemistry" (Grant ID Q0035, Welch Foundation)
  • "Pre-Clinical Development of Nuclease Mediated Gene Therapy for SCID" (Grant ID R01 AI097320, National Institute of Allergy and Infectious Diseases)
  • "Enhancing Training for Minority Biomedical Researchers" (Grant ID R25 GM056929, NIH National Institute of General Medical Sciences)
  • "Vision Research Core" (Grant ID P30 EY021721, NIH National Eye Institute)
  • "Trasnducin Interactions with Photoreceptor Membranes" (Grant ID R01 EY007981, NIH National Eye Institute)
  • "Rhodopsin Gene Correction and Gene Knockout in Rod Cells" (Grant ID R01 EY011731, NIH National Eye Institute)
SubmissionRegistration date: 28-Jul-2015
Baylor College of Medicine
RelevanceMedical
Project Data:
Resource NameNumber
of Links
Sequence data
SRA Experiments11
Other datasets
BioSample11
SRA Data Details
ParameterValue
Data volume, Gbases17
Data volume, Mbytes11665

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