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Cellosaurus XMDYYYi001-A (CVCL_A1ZV)

[Text version]

Cell line name XMDYYYi001-A
Synonyms BDU-iPSCs
Accession CVCL_A1ZV
Resource Identification Initiative To cite this cell line use: XMDYYYi001-A (RRID:CVCL_A1ZV)
Comments From: Department of Neurology, The First Affiliated Hospital of Xiamen University; Xiamen; China.
Population: Asian.
Derived from sampling site: Peripheral blood.
Sequence variations
  • Mutation; HGNC; 2928; DMD; Unexplicit; Ex2-19dup; Zygosity=Hemizygous (PubMed=33799273).
Disease Becker's muscular dystrophy (NCIt: C84587)
Becker muscular dystrophy (ORDO: Orphanet_98895)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 44Y
Category Induced pluripotent stem cell

PubMed=33799273; DOI=10.1016/j.scr.2021.102298
Wang D., Lin J.-J., Jin M., Wang N.
Establishment of a human iPSC line XMDYYYi001-A from a patient with Becker muscular dystrophy harboring duplications of exons 2-19 in dystrophin gene.
Stem Cell Res. 53:102298-102298(2021)

Cell line databases/resources hPSCreg; XMDYYYi001-A
Biological sample resources BioSamples; SAMEA7683945
Encyclopedic resources Wikidata; Q105511782
Entry history
Entry creation12-Jan-2021
Last entry update20-May-2021
Version number2