ID   GM13495
AC   CVCL_QX33
DR   CLO; CLO_0012301
DR   BioSample; SAMN00802440
DR   Coriell; GM13495
DR   Wikidata; Q54846581
RX   PubMed=35667217;
CC   Population: Caucasian.
CC   Sequence variation: Mutation; HGNC; 12796; WT1; Simple; p.Arg394Leu (c.181G>T); Zygosity=Heterozygous (PubMed=35667217).
CC   Derived from site: In situ; Testis, tunica albuginea; UBERON=UBERON_0006610.
CC   Cell type: Fibroblast; CL=CL_0000057.
DI   NCIt; C84668; Denys-Drash syndrome
DI   ORDO; Orphanet_220; Denys-Drash syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   1Y
CA   Finite cell line
DT   Created: 15-11-17; Last updated: 29-06-23; Version: 8
//
RX   PubMed=35667217; DOI=10.1016/j.scr.2022.102826;
RA   Doeser M.C., Krygin J., Ropke A., Han D., Wedlich-Soldner R.,
RA   Scholer H.R., Pavenstadt H., Kim K.-P.;
RT   "Generation of a human iPSC line (MPIi008-A) from a patient with
RT   Denys-Drash syndrome.";
RL   Stem Cell Res. 62:102826-102826(2022).
//