ID   WIBRe001-A-7
AC   CVCL_C7VS
SY   WIBR3_SNCA_A30P_A2-3; CALe002-A-7
DR   BioSamples; SAMEA114332307
DR   hPSCreg; WIBRe001-A-7
DR   Wikidata; Q123033913
RX   DOI=10.1101/2024.02.12.579917;
CC   Sequence variation: Mutation; HGNC; 11138; SNCA; Simple_edited; p.Ala30Pro (c.88G>C); ClinVar=VCV000014008; Zygosity=Heterozygous; Note=By prime editing (DOI=10.1101/2024.02.12.579917).
CC   Derived from site: In situ; Blastocyst; UBERON=UBERON_0000358.
CC   Cell type: Embryonic stem cell; CL=CL_0002322.
DI   NCIt; C198602; Parkinson disease 1, autosomal dominant
DI   ORDO; Orphanet_411602; Hereditary late-onset Parkinson disease
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_9767 ! WIBR3
SX   Female
AG   Blastocyst stage
CA   Embryonic stem cell
DT   Created: 29-06-23; Last updated: 02-05-24; Version: 4
//
RX   DOI=10.1101/2024.02.12.579917;
RA   Busquets Figueras O., Li H.-Q., Syed K.M., Alvarez Jerez P.,
RA   Dunnack J., Lo Bu R., Verma Y., Pangilinan G.R., Martin A., Straub J.,
RA   Du Y.-X., Simon V.M., Poser S., Bush Z., Diaz J., Sahagun A., Gao J.-P.,
RA   Hernandez D.G., Levine K.S., Booth E.O., Bateup H.S., Rio D.C.,
RA   Hockemeyer D., Blauwendraat C., Soldner F.F.;
RT   "iSCORE-PD: an isogenic stem cell collection to research Parkinson
RT   disease.";
RL   bioRxiv 2024:02.12.579917-02.12.579917(2024).
//