ID   STBCi084-A
AC   CVCL_RD30
SY   SFC871-03-12
DR   BioSamples; SAMEA104493859
DR   EBiSC; STBCi084-A
DR   ECACC; 66540840
DR   hPSCreg; STBCi084-A
DR   Wikidata; Q54970181
CC   From: StemBANCC; Oxford; United Kingdom.
CC   Sequence variation: Mutation; HGNC; HGNC:4177; GBA1; Simple; p.Asn409Ser (c.1226A>G) (N370S); ClinVar=VCV000004290; Zygosity=Unspecified (EBiSC=STBCi084-A).
CC   Discontinued: ECACC; 66540840; true.
CC   Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C26845; Parkinson disease
DI   ORDO; Orphanet_411602; Hereditary late-onset Parkinson disease
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_A8Z2 ! SF871
SX   Female
AG   Age unspecified
CA   Induced pluripotent stem cell
DT   Created: 05-03-18; Last updated: 10-04-25; Version: 16
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