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Cellosaurus SDQLCHi007-A (CVCL_XJ79)

[Text version]

Cell line name SDQLCHi007-A
Accession CVCL_XJ79
Resource Identification Initiative To cite this cell line use: SDQLCHi007-A (RRID:CVCL_XJ79)
Comments From: Qilu Children's Hospital of Shandong University; Jinan; China.
Derived from sampling site: Peripheral blood.
Sequence variations
  • Mutation; HGNC; 2928; DMD; Unexplicit; Ex49-50del; Zygosity=Hemizygous (PubMed=31812072).
Disease Duchenne muscular dystrophy (NCIt: C75482)
Duchenne muscular dystrophy (ORDO: Orphanet_98896)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 4Y7M
Category Induced pluripotent stem cell
Publications

PubMed=31812072; DOI=10.1016/j.scr.2019.101666
Guan J.-Y., Liu X.-N., Zhang H.-Y., Yang X.-M., Ma Y.-Y., Li Y., Gai Z.-T., Liu Y.
Reprogramming of human peripheral blood mononuclear cell (PBMC) from a Chinese patient suffering Duchenne muscular dystrophy to iPSC line (SDQLCHi007-A) carrying deletion of 49-50 exons in the DMD gene.
Stem Cell Res. 42:101666-101666(2020)

Cross-references
Cell line databases/resources hPSCreg; SDQLCHi007-A
SKIP; SKIP005646
Encyclopedic resources Wikidata; Q98129458
Entry history
Entry creation19-Dec-2019
Last entry update20-May-2021
Version number5