ID   STBCi007-B
AC   CVCL_RB42
SY   SFC855-03-08
DR   BioSamples; SAMEA104615901
DR   EBiSC; STBCi007-B
DR   ECACC; 66540909
DR   hPSCreg; STBCi007-B
DR   Wikidata; Q54956339
CC   From: StemBANCC; Oxford; United Kingdom.
CC   Sequence variation: Mutation; HGNC; 18618; LRRK2; Simple; p.Gly2019Ser (c.6055G>A); ClinVar=VCV000001940; Zygosity=Unspecified (EBiSC=STBCi007-B).
CC   Discontinued: ECACC; 66540909; 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)
OI   CVCL_RB41 ! STBCi007-A
OI   CVCL_RB43 ! STBCi007-C
SX   Male
AG   Age unspecified
CA   Induced pluripotent stem cell
DT   Created: 05-03-18; Last updated: 30-01-24; Version: 12
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