ID   UKWNLi007-B
AC   CVCL_C6TB
SY   FD1210/2
DR   BioSamples; SAMEA112262708
DR   hPSCreg; UKWNLi007-B
DR   Wikidata; Q117704934
RX   PubMed=36640471;
CC   From: Department of Neurology, University of Wurzburg; Wurzburg; Germany.
CC   Population: Caucasian.
CC   Sequence variation: Mutation; HGNC; 4296; GLA; Simple; p.Cys172Tyr (c.515G>A); ClinVar=VCV001323002; Zygosity=Hemizygous (PubMed=36640471).
CC   Derived from site: In situ; Leg, skin, dermis; UBERON=UBERON_0001511+UBERON_0002067.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C84701; Fabry disease
DI   ORDO; Orphanet_324; Fabry disease
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_C0H4 ! UKWNLi007-A
SX   Male
AG   34Y
CA   Induced pluripotent stem cell
DT   Created: 21-03-23; Last updated: 05-10-23; Version: 3
//
RX   PubMed=36640471; DOI=10.1016/j.scr.2023.103025;
RA   Klug K., Breyer M., Klopocki E., Uceyler N.;
RT   "Generation of two induced pluripotent stem cell lines UKWNLi006 and
RT   UKWNLi007 derived from two patients with an active site GLA mutation
RT   leading to a pain and no pain phenotype in Fabry disease.";
RL   Stem Cell Res. 67:103025-103025(2023).
//