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Cellosaurus CENSOi026-B (CVCL_WP25)

[Text version]
Cell line name CENSOi026-B
Synonyms F199c2
Accession CVCL_WP25
Resource Identification Initiative To cite this cell line use: CENSOi026-B (RRID:CVCL_WP25)
Comments From: Axol Bioscience Ltd. (Censo Biotechnologies); Cambridge; United Kingdom.
Cell type: Fibroblast; CL=CL_0000057.
Sequence variations
  • Mutation; HGNC; HGNC:14581; PINK1; Simple; p.Arg246Ter (c.736C>T); ClinVar=VCV000002407; Zygosity=Heterozygous (from autologous cell line CENSOi026-C).
  • Mutation; HGNC; HGNC:8607; PRKN; Unexplicit; Ex4-6 del; Zygosity=Heterozygous (from autologous cell line CENSOi026-C).
Disease Parkinson disease 2, autosomal recessive juvenile (NCIt: C198603)
Parkinson disease 6, early onset (NCIt: C184990)
Young-onset Parkinson disease (ORDO: Orphanet_2828)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_WP24 ! CENSOi026-A
CVCL_WP26 ! CENSOi026-C
Sex of cell Male
Age at sampling 58Y
Category Induced pluripotent stem cell
Cross-references
Cell line databases/resources hPSCreg; CENSOi026-B
Encyclopedic resources Wikidata; Q93446724
Entry history
Entry creation05-Jul-2019
Last entry update19-Dec-2024
Version number5