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Cellosaurus HPS1605 (CVCL_A3GN)

[Text version]
Cell line name HPS1605
Accession CVCL_A3GN
Resource Identification Initiative To cite this cell line use: HPS1605 (RRID:CVCL_A3GN)
Comments Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Disease Lennox-Gastaut syndrome (NCIt: C84816)
Lennox-Gastaut syndrome (ORDO: Orphanet_2382)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_A3GL ! HPS1603
CVCL_A3GM ! HPS1604
CVCL_A3GP ! HPS1606
CVCL_A3GQ ! HPS1607
CVCL_A3GR ! HPS1608
Sex of cell Male
Age at sampling 20-29Y
Category Induced pluripotent stem cell
Cross-references
Cell line collections (Providers) RCB; HPS1605
Encyclopedic resources Wikidata; Q105508211
Entry history
Entry creation12-Jan-2021
Last entry update29-Jun-2023
Version number4