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Cellosaurus GM21867 (CVCL_HL32)

[Text version]
Cell line name GM21867
Accession CVCL_HL32
Resource Identification Initiative To cite this cell line use: GM21867 (RRID:CVCL_HL32)
Comments Transformant: NCBI_TaxID; 10376; Epstein-Barr virus (EBV).
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
  • Mutation; HGNC; HGNC:12731; WAS; Simple; c.449+5G>A (IVS6+5G>A); Zygosity=Unspecified; Note=Activates a cryptic splice site (Coriell=GM21867).
Disease Wiskott-Aldrich syndrome (NCIt: C3448)
Wiskott-Aldrich syndrome (ORDO: Orphanet_906)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling Age unspecified
Category Transformed cell line
Cross-references
Cell line collections (Providers) Coriell; GM21867
Encyclopedic resources Wikidata; Q54852189
Entry history
Entry creation01-Dec-2016
Last entry update19-Dec-2024
Version number11