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Cellosaurus HPS1656 (CVCL_C9RW)

Cell line name HPS1656
Accession CVCL_C9RW
Resource Identification Initiative To cite this cell line use: HPS1656 (RRID:CVCL_C9RW)
Comments Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
  • Mutation; HGNC; 14270; PCDH19; Unexplicit; Not described; Zygosity=Unspecified (RCB=HPS1656).
Disease Developmental and epileptic encephalopathy 9 (NCIt: C201590)
Female restricted epilepsy with intellectual disability (ORDO: Orphanet_101039)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_C9RV ! HPS1655
CVCL_C9RX ! HPS1657
CVCL_C9RY ! HPS1658
CVCL_C9RZ ! HPS1659
CVCL_C9S0 ! HPS1660
Sex of cell Female
Age at sampling 10-19Y
Category Induced pluripotent stem cell
Cross-references
Cell line collections (Providers) RCB; HPS1656
Encyclopedic resources Wikidata; Q123031912
Entry history
Entry creation05-Oct-2023
Last entry update30-Jan-2024
Version number2