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Cellosaurus HyCyte CT26 mKRAS_p.G12C_c.558G＞T cell line (CVCL_F4KT)

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Cell line name HyCyte CT26 mKRAS_p.G12C_c.558G＞T cell line
Synonyms hSRSF2_p.P95H_c.284C＞A cell line
Accession CVCL_F4KT
Resource Identification Initiative To cite this cell line use: HyCyte CT26 mKRAS_p.G12C_c.558G＞T cell line (RRID:CVCL_F4KT)
Comments Population: Japanese.
Doubling time: 24-36 hours (Hysigen=CGMU-M2131).
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
  • Gene fusion; HGNC; HGNC:2457; CSNK2A1 + HGNC; HGNC:13917; DDX39B; Name(s)=CSNK2A1-DDX39B (from parent cell line).
  • Gene fusion; HGNC; HGNC:7132; KMT2A + HGNC; HGNC:7136; MLLT3; Name(s)=KMT2A-MLLT3, MLL-MLLT3, MLL-AF9 (from parent cell line).
  • Mutation; HGNC; HGNC:7989; NRAS; Simple; p.Gly12Asp (c.35G>A); ClinVar=VCV000039648; Zygosity=Heterozygous (from parent cell line).
  • Mutation; HGNC; HGNC:10783; SRSF2; Simple_edited; p.P95H (NM_001195427.2:c.284C>A); Zygosity=Heterozygous (Hysigen=CGMU-M2131).
  • Mutation; HGNC; HGNC:10783; SRSF2; Simple_edited; p.P96P (NM_001195427.2:c.285C>T NM_001195427.2:c.288G>T); Zygosity=Heterozygous; Note=Synonymous mutation (Hysigen=CGMU-M2131).
  • Mutation; HGNC; HGNC:11998; TP53; Simple; p.Arg174fs*3 (c.520_545del26); Zygosity=Heterozygous (from parent cell line).
Disease Childhood acute monocytic leukemia (NCIt: C9163)
Acute monoblastic/monocytic leukemia (ORDO: Orphanet_514)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_0006 (THP-1)
Sex of cell Male
Age at sampling 1Y
Category Cancer cell line
Cross-references
Cell line collections (Providers) Hysigen; CGMU-M2131
Entry history
Entry creation25-Jun-2026
Last entry update25-Jun-2026
Version number1