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Cellosaurus HyCyte CT26 mKRAS_p.G12C_c.572G＞T cell line (CVCL_F4L0)

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Cell line name HyCyte CT26 mKRAS_p.G12C_c.572G＞T cell line
Synonyms hFOXG1_c.256dupC cell line
Accession CVCL_F4L0
Resource Identification Initiative To cite this cell line use: HyCyte CT26 mKRAS_p.G12C_c.572G＞T cell line (RRID:CVCL_F4L0)
Comments Population: Caucasian.
Doubling time: 24-36 hours (Hysigen=CGMU-M2128).
Derived from site: In situ; Brain, parietal lobe; UBERON=UBERON_0001872.
Sequence variations
  • Mutation; HGNC; HGNC:3811; FOXG1; Simple_edited; NM_005249.5:c.246G>A NM_005249.5:c.249G>A NM_005249.5:c.252C>T NM_005249.5:c.255C>T; Zygosity=Homozygous; Note=Synonymous mutation (Hysigen=CGMU-M2128).
  • Mutation; HGNC; HGNC:3811; FOXG1; Simple_edited; NM_005249.5:c.256dupC; Zygosity=Homozygous (Hysigen=CGMU-M2128).
  • Mutation; HGNC; HGNC:5382; IDH1; None_reported; -; Zygosity=- (from parent cell line).
  • Mutation; HGNC; HGNC:9588; PTEN; Simple; p.Glu242Valfs*15 (c.723_724dupTG); ClinVar=VCV000536553; Zygosity=Unspecified (from parent cell line).
  • Mutation; HGNC; HGNC:11730; TERT; Simple; c.1-124C>T (c.228C>T) (C228T); Zygosity=Unspecified; Note=In promoter (from parent cell line).
  • Mutation; HGNC; HGNC:11998; TP53; Simple; p.Arg273His (c.818G>A); ClinVar=VCV000012366; Zygosity=Homozygous (from parent cell line).
Disease Astrocytoma (NCIt: C60781)
Astrocytoma (ORDO: Orphanet_94)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_0021 (U-251MG)
Sex of cell Male
Age at sampling 75Y
Category Cancer cell line
Cross-references
Cell line collections (Providers) Hysigen; CGMU-M2128
Entry history
Entry creation25-Jun-2026
Last entry update25-Jun-2026
Version number1