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Accession: PRJNA294630 ID: 294630

Homo sapiens (human)

Identification of Potentially Pathogenic Variants in the Posterior Polymorphous Corneal Dystrophy 1 Locus

See Genome Information for Homo sapiens
Purpose: To identify the genetic basis of posterior polymorphous corneal dystrophy 1 (PPCD1). More...
AccessionPRJNA294630; GEO: GSE72617
Data TypeVariation
ScopeMultiisolate
OrganismHomo sapiens[Taxonomy ID: 9606]
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
PublicationsLe DJ et al., "Identification of Potentially Pathogenic Variants in the Posterior Polymorphous Corneal Dystrophy 1 Locus.", PLoS One, 2016;11(6):e0158467
Grants
  • "Identification and Characterization of the Genetic Basis of PPCD" (Grant ID R01 EY022082, NIH National Eye Institute)
SubmissionRegistration date: 1-Sep-2015
Cornea Genetics Laboratory, Ophthalmology, Stein Eye Institute, UCLA
RelevanceMedical
Project Data:
Resource NameNumber
of Links
Publications
PubMed1
PMC1
Other datasets
GEO DataSets1
GEO Data Details
ParameterValue
Data volume, Spots440608
Data volume, Processed Mbytes12
Data volume, Supplementary Mbytes140

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  • Homo sapiens
    Homo sapiens
    Identification of Potentially Pathogenic Variants in the Posterior Polymorphous Corneal Dystrophy 1 Locus
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