ID   ZJUi005-A [Wrong name]
AC   CVCL_A0ZZ
SY   WXG-iPSC-C6
DR   Wikidata; Q108821561
RX   PubMed=34298435;
CC   From: Women's Hospital, Zhejiang University School of Medicine; Hangzhou; China.
CC   Sequence variation: Mutation; HGNC; HGNC:3603; FBN1; Simple; p.Cys2245Tyr (c.6734G>A); ClinVar=VCV000968455; Zygosity=Heterozygous (PubMed=34298435).
CC   Caution: There are 2 cell lines generated by the same group with the same name. This cell line should be renamed.
CC   Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C34807; Marfan syndrome
DI   ORDO; Orphanet_558; Marfan syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   47Y
CA   Induced pluripotent stem cell
DT   Created: 23-09-21; Last updated: 19-12-24; Version: 6
//
RX   PubMed=34298435; DOI=10.1016/j.scr.2021.102459;
RA   Pan Z.-W., Wang H.-K., Wang H., Liu Y., Liang P.;
RT   "Generation of an induced pluripotent stem cell line from a patient
RT   carrying FBN1/c.6734 G > A mutation.";
RL   Stem Cell Res. 55:102459-102459(2021).
//