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Cellosaurus INSRMi002-A (CVCL_WN90)

[Text version]
Cell line name INSRMi002-A
Synonyms PC117_c2
Accession CVCL_WN90
Resource Identification Initiative To cite this cell line use: INSRMi002-A (RRID:CVCL_WN90)
Comments From: INSERM; Paris; France.
Population: Caucasian.
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
  • Mutation; HGNC; HGNC:18423; DEPDC5; Simple; p.Glu1420Argfs*153 (c.4260delG); Zygosity=Heterozygous (hPSCreg=INSRMi002-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 30-34Y
Category Induced pluripotent stem cell
Cross-references
Cell line databases/resources hPSCreg; INSRMi002-A
Biological sample resources BioSamples; SAMEA5794618
Encyclopedic resources Wikidata; Q94318176
Entry history
Entry creation05-Jul-2019
Last entry update19-Dec-2024
Version number8