ID   STBCi019-B
AC   CVCL_RB72
SY   SFC828-03-09
DR   BioSamples; SAMEA104493639
DR   EBiSC; STBCi019-B
DR   ECACC; 66540677
DR   hPSCreg; STBCi019-B
DR   Wikidata; Q54956389
CC   From: StemBANCC; Oxford; United Kingdom.
CC   Sequence variation: Mutation; HGNC; 11138; SNCA; Simple; p.Ala53Thr (c.157G>A); ClinVar=VCV000014007; Zygosity=Heterozygous (EBiSC=STBCi019-B).
CC   Discontinued: EBiSC; STBCi019-B; true.
CC   Discontinued: ECACC; 66540677; true.
CC   Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C198602; Parkinson disease 1, autosomal dominant
DI   ORDO; Orphanet_411602; Hereditary late-onset Parkinson disease
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_A8X7 ! SF828
SX   Female
AG   51Y
CA   Induced pluripotent stem cell
DT   Created: 05-03-18; Last updated: 30-01-24; Version: 12
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