ID   PB(DF)
AC   CVCL_ZX89
SY   DF(PB); PB(Dermal Fibroblast)
DR   Wikidata; Q102114735
CC   Sequence variation: Mutation; HGNC; HGNC:8607; PRKN; Unexplicit; Ex6-7del; Zygosity=Homozygous (from child cell lines PB1; PB2; PB18; PB20).
CC   Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C198603; Parkinson disease 2, autosomal recessive juvenile
DI   ORDO; Orphanet_2828; Young-onset Parkinson disease
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_ZX88 ! PB(LCL)
OI   CVCL_ZX90 ! PB(T-cell)
SX   Male
AG   50Y
CA   Finite cell line
DT   Created: 29-10-20; Last updated: 19-12-24; Version: 8
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