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Cellosaurus HCT 116 CTNNB1(+/-) (CVCL_HD74)
[Text version]
Cell line name |
HCT 116 CTNNB1(+/-)
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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.
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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; 3373; EP300; Simple; p.Met1470Cysfs*22 (c.4408delA); Zygosity=Heterozygous (from parent cell line).
- Mutation; HGNC; 3373; EP300; Simple; p.Asn1700Thrfs*9 (c.5099delA); 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).
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Disease |
Colon carcinoma (NCIt: C4910)
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Species of origin |
Homo sapiens (Human)
(NCBI Taxonomy: 9606)
|
Hierarchy |
Parent: CVCL_0291 (HCT 116)
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Sex of cell |
Male
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Age at sampling |
48Y
|
Category |
Cancer cell line
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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
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Encyclopedic resources |
Wikidata; Q54881928
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Entry history |
Entry creation | 01-Dec-2016 |
Last entry update | 23-Jun-2022 |
Version number | 11 |
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