ID   STBCi088-C
AC   CVCL_RD43
SY   SFC872-03-03
DR   BioSamples; SAMEA104493881
DR   EBiSC; STBCi088-C
DR   ECACC; 66540853
DR   hPSCreg; STBCi088-C
DR   Wikidata; Q54970196
CC   From: StemBANCC; Oxford; United Kingdom.
CC   Sequence variation: Mutation; HGNC; HGNC:4177; GBA1; Simple; p.Leu483Pro (c.1448T>C) (L444P); ClinVar=VCV000004288; Zygosity=Unspecified (EBiSC=STBCi088-C).
CC   Discontinued: ECACC; 66540853; true.
CC   Cell type: Fibroblast; CL=CL_0000057.
DI   NCIt; C26845; Parkinson disease
DI   ORDO; Orphanet_411602; Hereditary late-onset Parkinson disease
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_RD41 ! STBCi088-A
OI   CVCL_RD42 ! STBCi088-B
SX   Male
AG   Age unspecified
CA   Induced pluripotent stem cell
DT   Created: 05-03-18; Last updated: 10-04-25; Version: 15
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