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Cellosaurus NCKDi002-A (CVCL_A5FS)

[Text version]

Cell line name NCKDi002-A
Synonyms NCKD-iPS-FSGS-WT1-002
Accession CVCL_A5FS
Resource Identification Initiative To cite this cell line use: NCKDi002-A (RRID:CVCL_A5FS)
Comments From: National Center of Kidney Diseases; Nanjing; China.
Population: Chinese; Han.
Derived from sampling site: Peripheral blood.
Sequence variations Mutation; HGNC; 12796; WT1; Simple; p.Arg363Gly (c.1087A>G) (p.Arg219Gly, c.655A>G); Zygosity=Heterozygous (PubMed=33780729).
Disease Nephrotic syndrome - WT1 associated (NCIt: C123106)
Genetic steroid-resistant nephrotic syndrome (ORDO: Orphanet_656)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 22Y
Category Induced pluripotent stem cell
Publications

PubMed=33780729; DOI=10.1016/j.scr.2021.102293
Wu H.-D., Wang G., Gao E.-Z., Zhao J., Zhang L., Chen L., Zhu Y.-Q., Zhang J., Liu Z.-H.
Generation of the induced pluripotent stem cell line (NCKDi002-A) from a 22-year-old patient with focal segmental glomerular sclerosis carrying a heterozygous mutation in WT1 gene.
Stem Cell Res. 53:102293-102293(2021)

Cross-references
Cell line databases/resources hPSCreg; NCKDi002-A
Other Wikidata; Q107116541
Entry history
Entry creation20-May-2021
Last entry update23-Sep-2021
Version number2