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Cellosaurus PFIZi019-A (CVCL_RF98)

[Text version]
Cell line name PFIZi019-A
Synonyms BC145c6; RCi202
Accession CVCL_RF98
Resource Identification Initiative To cite this cell line use: PFIZi019-A (RRID:CVCL_RF98)
Comments From: Pfizer, Inc.; New York; USA.
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
  • Mutation; HGNC; 10585; SCN1A; Simple; p.Tyr1508fs (c.4522delT); Zygosity=Heterozygous (EBiSC=PFIZi019-A).
Disease Developmental and epileptic encephalopathy 6A (NCIt: C147071)
Dravet syndrome (ORDO: Orphanet_33069)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 5-9Y
Category Induced pluripotent stem cell
Cross-references
Cell line collections (Providers) EBiSC; PFIZi019-A
ECACC; 66540420 - Discontinued
Cell line databases/resources hPSCreg; PFIZi019-A
Biological sample resources BioSamples; SAMEA4458852
Encyclopedic resources Wikidata; Q54947274
Entry history
Entry creation05-Mar-2018
Last entry update30-Jan-2024
Version number12