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Cellosaurus HCT 116 CTNNB1(+/-) (CVCL_HD74)

[Text version]

Cell line name HCT 116 CTNNB1(+/-)
Synonyms CTNNB1 (+/-) HCT116; CTNNB1 WT/- HCT116
Accession CVCL_HD74
Resource Identification Initiative To cite this cell line use: HCT 116 CTNNB1(+/-) (RRID:CVCL_HD74)
Comments Characteristics: In HCT 116 one of the two CTNNB1 alleles has a 3-bp deletion that eliminates S-45. This cell line is KO for the mutant allele.
Knockout cell: Method=Homologous recombination (1 of 2 alleles); HGNC; 2514; CTNNB1.
Derived from sampling site: Colon.
Sequence variations Mutation; HGNC; 173; ACVR2A; Simple; p.Lys437Argfs*5 (c.1310delA); dbSNP=rs764719749; Zygosity=Homozygous (from parent cell line).
Mutation; HGNC; 1101; BRCA2; Simple; p.Ile2675Aspfs*6 (c.8021dupA) (c.8021_8022insA); ClinVar=VCV000267050; Zygosity=Heterozygous (from parent cell line).
Mutation; HGNC; 1787; CDKN2A; Simple; p.Arg24Serfs*20 (c.68dupG) (c.68_69insG) (p.G23fs); Zygosity=Heterozygous (from parent cell line).
Mutation; HGNC; 6407; KRAS; Simple; p.Gly13Asp (c.38G>A); ClinVar=VCV000012580; Zygosity=Heterozygous (from parent cell line).
Mutation; HGNC; 8975; PIK3CA; Simple; p.His1047Arg (c.3140A>G); ClinVar=VCV000013652; Zygosity=Heterozygous (from parent cell line).
Mutation; HGNC; 11773; TGFBR2; Simple; p.Lys128Serfs*35 (c.383delA); ClinVar=VCV000477546; Zygosity=Homozygous (from parent cell line).
Disease Colon carcinoma (NCIt: C4910)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_0291 (HCT 116)
Sex of cell Male
Age at sampling 48Y
Category Cancer cell line
Publications

PubMed=12060769; DOI=10.1073/pnas.082240999
Chan T.A., Wang Z.-H., Dang L.H., Vogelstein B., Kinzler K.W.
Targeted inactivation of CTNNB1 reveals unexpected effects of beta-catenin mutation.
Proc. Natl. Acad. Sci. U.S.A. 99:8265-8270(2002)

Cross-references
Cell line collections Horizon_Discovery; HD+104-009
Other Wikidata; Q54881928
Entry history
Entry creation01-Dec-2016
Last entry update20-May-2021
Version number10