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Cellosaurus SHCMDLi001-A (CVCL_A8PJ)

[Text version]

Cell line name SHCMDLi001-A
Accession CVCL_A8PJ
Resource Identification Initiative To cite this cell line use: SHCMDLi001-A (RRID:CVCL_A8PJ)
Comments From: Shanghai Children's Hospital; Shanghai; China.
Population: Chinese; Han.
Derived from sampling site: Peripheral blood.
Sequence variations
  • Mutation; HGNC; 20456; TRAF7; Simple; p.Arg655Gln (c.1964G>A); ClinVar=VCV000587685; Zygosity=Heterozygous; Note=De novo mutation (PubMed=34088006).
Disease Cardiac, facial, and digital anomalies with developmental delay (NCIt: C179868)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling 12Y
Category Induced pluripotent stem cell

PubMed=34088006; DOI=10.1016/j.scr.2021.102377
Song X.-Z., Feng J.-C., Lan X.-P., Tang X.-J., Xu W.-H., Shen J., Yu G.-J., Jia J., Zhang H., Lu Q., Wu S.-N.
Generation and characterization of an iPSC line (SHCMDLi001-A) from a 12-year-old Chinese Han patient with TRAF7 syndrome and of an iPSC line (SHCMDLi002-A) from a control individual.
Stem Cell Res. 53:102377-102377(2021)

Cell line databases/resources hPSCreg; SHCMDLi001-A
Encyclopedic resources Wikidata; Q108821300
Entry history
Entry creation23-Sep-2021
Last entry update16-Dec-2021
Version number2