ID   STBCi005-B
AC   CVCL_RB38
SY   SFC833-03-05
DR   BioSamples; SAMEA104615893
DR   EBiSC; STBCi005-B
DR   ECACC; 66540907
DR   hPSCreg; STBCi005-B
DR   Wikidata; Q54956330
CC   From: StemBANCC; Oxford; United Kingdom.
CC   Sequence variation: Mutation; HGNC; HGNC:18618; LRRK2; Simple; p.Gly2019Ser (c.6055G>A); ClinVar=VCV000001940; Zygosity=Unspecified (EBiSC=STBCi005-B).
CC   Discontinued: ECACC; 66540907; 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_RB37 ! STBCi005-A
OI   CVCL_RB39 ! STBCi005-C
SX   Male
AG   Age unspecified
CA   Induced pluripotent stem cell
DT   Created: 05-03-18; Last updated: 19-12-24; Version: 13
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