ID   NCKDi002-A
AC   CVCL_A5FS
SY   NCKD-iPS-FSGS-WT1-002
DR   hPSCreg; NCKDi002-A
DR   Wikidata; Q107116541
RX   PubMed=33780729;
CC   From: National Center of Kidney Diseases; Nanjing; China.
CC   Population: Chinese; Han.
CC   Sequence variation: Mutation; HGNC; 12796; WT1; Simple; p.Arg363Gly (c.1087A>G) (p.Arg219Gly, c.655A>G); Zygosity=Heterozygous (PubMed=33780729).
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
DI   NCIt; C123106; Nephrotic syndrome - WT1 associated
DI   ORDO; Orphanet_656; Genetic steroid-resistant nephrotic syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   22Y
CA   Induced pluripotent stem cell
DT   Created: 20-05-21; Last updated: 29-06-23; Version: 4
//
RX   PubMed=33780729; DOI=10.1016/j.scr.2021.102293;
RA   Wu H.-D., Wang G., Gao E.-Z., Zhao J., Zhang L., Chen L., Zhu Y.-Q.,
RA   Zhang J., Liu Z.-H.;
RT   "Generation of the induced pluripotent stem cell line (NCKDi002-A)
RT   from a 22-year-old patient with focal segmental glomerular sclerosis
RT   carrying a heterozygous mutation in WT1 gene.";
RL   Stem Cell Res. 53:102293-102293(2021).
//