ID   STBCi042-B
AC   CVCL_RC27
SY   SFC848-03-04
DR   BioSamples; SAMEA104493712
DR   EBiSC; STBCi042-B
DR   ECACC; 66540736
DR   hPSCreg; STBCi042-B
DR   Wikidata; Q54956469
CC   From: StemBANCC; Oxford; United Kingdom.
CC   Sequence variation: Mutation; HGNC; 4177; GBA1; Simple; p.Asn409Ser (c.1226A>G) (N370S); ClinVar=VCV000004290; Zygosity=Unspecified (EBiSC=STBCi042-B).
CC   Discontinued: ECACC; 66540736; 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's disease
DI   ORDO; Orphanet_411602; Hereditary late-onset Parkinson disease
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_A8Z3 ! SF848
SX   Male
AG   Age unspecified
CA   Induced pluripotent stem cell
DT   Created: 05-03-18; Last updated: 30-01-24; Version: 14
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