ID   HyCyte CT26 mKRAS_p.G12C_c.558G＞T cell line
AC   CVCL_F4KT
SY   hSRSF2_p.P95H_c.284C＞A cell line
DR   Hysigen; CGMU-M2131
CC   Population: Japanese.
CC   Doubling time: 24-36 hours (Hysigen=CGMU-M2131).
CC   Sequence variation: Gene fusion; HGNC; HGNC:2457; CSNK2A1 + HGNC; HGNC:13917; DDX39B; Name(s)=CSNK2A1-DDX39B (from parent cell line).
CC   Sequence variation: Gene fusion; HGNC; HGNC:7132; KMT2A + HGNC; HGNC:7136; MLLT3; Name(s)=KMT2A-MLLT3, MLL-MLLT3, MLL-AF9 (from parent cell line).
CC   Sequence variation: Mutation; HGNC; HGNC:7989; NRAS; Simple; p.Gly12Asp (c.35G>A); ClinVar=VCV000039648; Zygosity=Heterozygous (from parent cell line).
CC   Sequence variation: Mutation; HGNC; HGNC:10783; SRSF2; Simple_edited; p.P95H (NM_001195427.2:c.284C>A); Zygosity=Heterozygous (Hysigen=CGMU-M2131).
CC   Sequence variation: 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).
CC   Sequence variation: Mutation; HGNC; HGNC:11998; TP53; Simple; p.Arg174fs*3 (c.520_545del26); Zygosity=Heterozygous (from parent cell line).
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
DI   NCIt; C9163; Childhood acute monocytic leukemia
DI   ORDO; Orphanet_514; Acute monoblastic/monocytic leukemia
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_0006 ! THP-1
SX   Male
AG   1Y
CA   Cancer cell line
DT   Created: 25-06-26; Last updated: 25-06-26; Version: 1
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