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Cellosaurus INSRMi006-A (CVCL_WR06)

[Text version]
Cell line name INSRMi006-A
Synonyms PC131_c8
Accession CVCL_WR06
Resource Identification Initiative To cite this cell line use: INSRMi006-A (RRID:CVCL_WR06)
Comments From: INSERM; Paris; France.
Population: Caucasian.
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
  • Mutation; HGNC; 18423; DEPDC5; Simple; p.Glu1385Ter (c.4151_4152insC); Zygosity=Heterozygous (hPSCreg=INSRMi006-A).
Disease Familial focal epilepsy with variable foci 1 (NCIt: C161005)
Familial focal epilepsy with variable foci (ORDO: Orphanet_98820)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 20-24Y
Category Induced pluripotent stem cell
Cell line databases/resources hPSCreg; INSRMi006-A
Biological sample resources BioSamples; SAMEA5829798
Encyclopedic resources Wikidata; Q94318194
Entry history
Entry creation05-Jul-2019
Last entry update29-Jun-2023
Version number7