ID   STBCi026-A-3
AC   CVCL_A9A0
SY   SFC840-03-03 LRRK2 WT/R1441C H3
DR   BioSamples; SAMEA5859481
DR   EBiSC; STBCi026-A-3
DR   ECACC; 66541207
DR   hPSCreg; STBCi026-A-3
DR   Wikidata; Q102114947
CC   From: StemBANCC; Oxford; United Kingdom.
CC   Sequence variation: Mutation; HGNC; HGNC:18618; LRRK2; Simple_edited; p.Arg1441Cys (c.4321C>T); ClinVar=VCV000001938; Zygosity=Heterozygous; Note=By CRISPR/Cas9 (EBiSC=STBCi026-A-3).
CC   Discontinued: ECACC; 66541207; true.
CC   Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C198605; Parkinson disease 8, autosomal dominant
DI   ORDO; Orphanet_411602; Hereditary late-onset Parkinson disease
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_RB85 ! STBCi026-A
SX   Female
AG   67Y
CA   Induced pluripotent stem cell
DT   Created: 29-10-20; Last updated: 19-12-24; Version: 10
//