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Cellosaurus HPS1460 (CVCL_UN81)

[Text version]
Cell line name HPS1460
Accession CVCL_UN81
Resource Identification Initiative To cite this cell line use: HPS1460 (RRID:CVCL_UN81)
Comments Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
  • Mutation; HGNC; 10585; SCN1A; Unexplicit; Not described; Zygosity=Heterozygous (RCB=HPS1460).
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_YR62 ! HPS1461
CVCL_YR63 ! HPS1462
CVCL_YR64 ! HPS1463
CVCL_YR65 ! HPS1464
CVCL_YR66 ! HPS1465
Sex of cell Female
Age at sampling 6-9Y
Category Induced pluripotent stem cell
Cell line collections (Providers) RCB; HPS1460
Encyclopedic resources Wikidata; Q94219763
Entry history
Entry creation25-Feb-2019
Last entry update05-Oct-2023
Version number9