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Cellosaurus HPS2101 (CVCL_YR81)

[Text version]
Cell line name HPS2101
Accession CVCL_YR81
Resource Identification Initiative To cite this cell line use: HPS2101 (RRID:CVCL_YR81)
Comments Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
  • Mutation; HGNC; 10585; SCN1A; Unexplicit; Not described; Zygosity=Unspecified (RCB=HPS2101).
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_UN97 ! HPS2096
CVCL_YR77 ! HPS2097
CVCL_YR78 ! HPS2098
CVCL_YR79 ! HPS2099
CVCL_YR80 ! HPS2100
Sex of cell Female
Age at sampling 6-9Y
Category Induced pluripotent stem cell
Cross-references
Cell line collections (Providers) RCB; HPS2101
Encyclopedic resources Wikidata; Q94219932
Entry history
Entry creation12-Mar-2020
Last entry update05-Oct-2023
Version number8