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Accession: PRJNA283635 ID: 283635

Homo sapiens (human)

Homo sapiens Exome

See Genome Information for Homo sapiens
We describe targeted exon sequencing data derived from a case of atypical promyelocytic leukemia associated with a STAT5B-RARA fusion gene, as well as a small deletion in RARA exon 9 and a RARA R276W substitution that have been linked to resistance to all-trans retinoic acid. More...
AccessionPRJNA283635
Data TypeExome
ScopeMonoisolate
OrganismHomo sapiens[Taxonomy ID: 9606]
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
PublicationsKluk MJ et al., "Myeloid neoplasm demonstrating a STAT5B-RARA rearrangement and genetic alterations associated with all-trans retinoic acid resistance identified by a custom next-generation sequencing assay.", Cold Spring Harb Mol Case Stud, 2015 Oct;1(1):a000307
SubmissionRegistration date: 12-May-2015
Brigham and Women's Hospital
RelevanceMedical
Project Data:
Resource NameNumber
of Links
Sequence data
SRA Experiments1
Publications
PubMed1
PMC1
Other datasets
BioSample1
SRA Data Details
ParameterValue
Data volume, Gbases2
Data volume, Mbytes881

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