ID   STBCi004-C
AC   CVCL_RB36
SY   SFC832-03-07
DR   BioSamples; SAMEA104615895
DR   EBiSC; STBCi004-C
DR   ECACC; 66540906
DR   hPSCreg; STBCi004-C
DR   Wikidata; Q54956327
CC   From: StemBANCC; Oxford; United Kingdom.
CC   Sequence variation: Mutation; HGNC; 18618; LRRK2; Simple; p.Gly2019Ser (c.6055G>A); ClinVar=VCV000001940; Zygosity=Heterozygous (EBiSC=STBCi004-C).
CC   Discontinued: ECACC; 66540906; 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_RB34 ! STBCi004-A
OI   CVCL_RB35 ! STBCi004-B
SX   Female
AG   77Y
CA   Induced pluripotent stem cell
DT   Created: 05-03-18; Last updated: 30-01-24; Version: 12
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