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Cellosaurus HPS2838 (CVCL_YR97)

Cell line name HPS2838
Accession CVCL_YR97
Resource Identification Initiative To cite this cell line use: HPS2838 (RRID:CVCL_YR97)
Comments Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
  • Mutation; HGNC; 10585; SCN1A; Unexplicit; Not described; Zygosity=Unspecified (RCB=HPS2838).
Disease Developmental and epileptic encephalopathy 6A (NCIt: C147071)
Dravet syndrome (ORDO: Orphanet_33069)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_UP20 ! HPS2834
CVCL_YR94 ! HPS2835
CVCL_YR95 ! HPS2836
CVCL_YR96 ! HPS2837
CVCL_YR98 ! HPS2839
Sex of cell Female
Age at sampling 6-9Y
Category Induced pluripotent stem cell
Cross-references
Cell line collections (Providers) RCB; HPS2838
Encyclopedic resources Wikidata; Q94220283
Entry history
Entry creation12-Mar-2020
Last entry update05-Oct-2023
Version number8