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Cellosaurus PFIZi018-A (CVCL_RF97)

[Text version]
Cell line name PFIZi018-A
Synonyms BC143c8; RCi207
Accession CVCL_RF97
Resource Identification Initiative To cite this cell line use: PFIZi018-A (RRID:CVCL_RF97)
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.Arg1245Ter (c.3733C>T) (R1234*); ClinVar=VCV000167639; Zygosity=Heterozygous (EBiSC=PFIZi018-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 Female
Age at sampling 10-14Y
Category Induced pluripotent stem cell
Cell line collections (Providers) EBiSC; PFIZi018-A
ECACC; 66540419 - Discontinued
Cell line databases/resources hPSCreg; PFIZi018-A
Biological sample resources BioSamples; SAMEA4458850
Encyclopedic resources Wikidata; Q54947273
Entry history
Entry creation05-Mar-2018
Last entry update30-Jan-2024
Version number12