ID   FHUSTCi001-A
AC   CVCL_C0FQ
DR   BioSamples; SAMEA12056141
DR   hPSCreg; FHUSTCi001-A
DR   Wikidata; Q112929562
RX   PubMed=35395622;
CC   From: The First Affiliated Hospital of USTC, Division of life Science and Medicine, University of Science and Technology of China; Hefei; China.
CC   Population: Chinese; Han.
CC   Sequence variation: Mutation; HGNC; 3778; FN1; Simple; p.Val1868Met (c.5602G>A); ClinVar=VCV001051358; Zygosity=Heterozygous (PubMed=35395622).
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
DI   NCIt; C187984; Glomerulopathy with fibronectin deposits-2
DI   ORDO; Orphanet_84090; Fibronectin glomerulopathy
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   11Y
CA   Induced pluripotent stem cell
DT   Created: 23-06-22; Last updated: 29-06-23; Version: 4
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RX   PubMed=35395622; DOI=10.1016/j.scr.2022.102751;
RA   Yu X., Wang H.-T., Xiao F., Jiang S., Li K.-L., Chen Q.-X., Wang G.-S.,
RA   Kong F., Zhao S.-T.;
RT   "Generation of the integration-free induced pluripotent stem cell line
RT   (FHUSTCi001-A) from a patient with glomerulopathy with fibronectin
RT   deposits harboring FN1 mutation.";
RL   Stem Cell Res. 61:102751-102751(2022).
//