| Cell line name |
HCT116-EGFP |
| Accession |
CVCL_XE63 |
| Resource Identification Initiative |
To cite this cell line use: HCT116-EGFP (RRID:CVCL_XE63) |
| Comments |
Population: Caucasian. Genetic integration: Method=Transfection/transduction; Gene=FPbase; R9NL8; eGFP (Note=Enhanced GFP). Miscellaneous: Formerly the CCRID database had an entry describing this cell line (3111C0001CCC000661). It was the sole source of information for this entry. Derived from site: In situ; Colon; UBERON=UBERON_0001155. |
| Sequence variations |
- Mutation; HGNC; HGNC:173; ACVR2A; Simple; p.Lys437Argfs*5 (c.1310delA); dbSNP=rs764719749; Zygosity=Homozygous (from parent cell line).
- Mutation; HGNC; HGNC:1101; BRCA2; Simple; p.Ile2675Aspfs*6 (c.8021dupA) (c.8021_8022insA); ClinVar=VCV000267050; Zygosity=Heterozygous (from parent cell line).
- Mutation; HGNC; HGNC:1787; CDKN2A; Simple; p.Arg24Serfs*20 (c.68dupG) (c.68_69insG) (p.G23fs); Zygosity=Heterozygous (from parent cell line).
- Mutation; HGNC; HGNC:2514; CTNNB1; Simple; p.Ser45del (c.133_135delTCT); ClinVar=VCV000017576; Zygosity=Heterozygous (from parent cell line).
- Mutation; HGNC; HGNC:3373; EP300; Simple; p.Met1470Cysfs*22 (c.4408delA); Zygosity=Heterozygous (from parent cell line).
- Mutation; HGNC; HGNC:3373; EP300; Simple; p.Asn1700Thrfs*9 (c.5099delA); Zygosity=Heterozygous (from parent cell line).
- Mutation; HGNC; HGNC:6407; KRAS; Simple; p.Gly13Asp (c.38G>A); ClinVar=VCV000012580; Zygosity=Heterozygous (from parent cell line).
- Mutation; HGNC; HGNC:8975; PIK3CA; Simple; p.His1047Arg (c.3140A>G); ClinVar=VCV000013652; Zygosity=Heterozygous (from parent cell line).
- Mutation; HGNC; HGNC:9277; PPM1D; Simple; p.Leu450Ter (c.1349delT) (p.Leu450fs) (c.1344delT); Zygosity=Heterozygous (from parent cell line).
- Mutation; HGNC; 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 |
| STR profile |
Source(s): CCRID
Markers:| Amelogenin | X |
| CSF1PO | 7,10 |
| D2S1338 | 16 |
| D3S1358 | 12,19 |
| D5S818 | 10,11 |
| D6S1043 | 13 |
| D7S820 | 11,12 |
| D8S1179 | 12,14 |
| D12S391 | 17,21 |
| D13S317 | 10,12 |
| D16S539 | 11,13 |
| D18S51 | 17 |
| D19S433 | 12,13 |
| D21S11 | 29,30 |
| FGA | 18,23 |
| Penta E | 13,14 |
| TH01 | 8,9 |
| TPOX | 8 |
| vWA | 17,22 |
Run an STR similarity search on this cell line |
| Cross-references |
| Cell line databases/resources |
cancercelllines; CVCL_XE63
|
| Encyclopedic resources |
Wikidata; Q93985580
|
| Entry history |
| Entry creation | 06-Sep-2019 |
| Last entry update | 19-Dec-2024 |
| Version number | 11 |
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