Cell lines database

p53 database

p53 mutations in cell lines

The hanbook of p53 mutation in cell lines

Cell lines with a controversial p53 status

The NCI 60 panel

Bladder cancer cell lines

Brain cancer cell lines

Breast cancer cell lines

Cervical carcinoma

Colorectal cancer cell lines

Esophageal cancer cell lines

Gastric cancer cell lines

Head and Neck cancer cell lines

Leukemia / Lymphoma cell lines

NSCLC cancer cell lines

Ovarian cancer cell lines

Pancreatic cancer cell lines

Sarcoma cell lines

SCLC cancer cell lines

Melanoma cell lines

Hepatocellular carcinoma

References

Ovarian cancer

Table I : cell lines with wt p53

Cell line
ATCC
Reference
KGN  
2249
A2780  
2249
RMG-1  
2249
CH1  
925
LK1  
925
LK2  
925

 

Table II : cell lines with p53 gene deletion or rearrangement

No data

Table III : cell lines with p53 splice mutation
(exonic mutations that modify splice are listed in table IV)

No data

Table IV: cell lines with p53 mutations (missense or frameshift)
More information is available in the handbook

Pos: Codon position (1 to 393);
WT: Normal base sequence of the codon in which the mutation occurred;
Mut Sequence of the mutated codon. If the mutation is a deletion or an insertion, it is indicated by "del" or "ins" followed by the number of deleted or inserted bases. The position in the codon is indicated by “a”, “b”, or “c” for the first, second or third base of the codon respectively. Example: "del66b" is a deletion of 66 bases including the second base of the codon; "ins4a" is an insertion of 4 bases occurring between the first and the second base of the codon. Label a, b, or c is omitted if the boundary of the deletion or insertion is unknown
AA: Wild type amino acid;
Mut: Mutant amino acid. Stop: nonsense mutation: Fs.: Frameshift mutation: InF: In-frame insertion or deletion;
Comp: complexity of the mutation: SM: Single mutational event in the tumor; DMU (Double Mutation Unknown): Two p53 mutations in the same tumor but their allelique distribution is unknown; DMD (Double Mutation Different allele): Two p53 mutations in the same tumor on two different p53 alleles; DMS (Double Mutation Same allele): Two p53 mutations in the same tumor on the same p53 allele: MM (Multiple Mutation): More than two p53 mutations in the same tumor;
NB: Number of tumors with this particular mutant in the database;
Ref: reference number;
Comments: information;

Table of references (available also in the handbook)

Pos.
WT
Mut
      AA
Mut
Comp
Name
NB
Ref
Comments
99 TCC del2b Ser Fs. SM 6 1 376 Single report
316 CCC CCT Pro Pro SM 222 6 798 Single report
273 CGT CAT Arg His SM 2774 780 798 Single report
172 GTT TTT Val Phe SM 2780CP 19 963 Single report
193 CAT CTT His Leu SM A. P. 55 1011 Single report
172 GTT TTT Val Phe SM A2780-CP-20 19 798 Single report
196 CGA TGA Arg Stop SM C. P./1 241 1011 Single report
193 CAT CGT His Arg SM C. V. 86 1011 Single report
136 CAA TAA Gln Stop SM Caov-3 47 144 Single report
147 GTT GAT Val Asp SM Caov-4 7 144 Single report
213 CGA TGA Arg Stop SM DDL11 306 1011 Single report
124 TGC CGC Cys Arg SM EFO-21 4 2249 Mutation in COSMIC database
273 CGT TGT Arg Cys SM EFO-27 687 2249 Mutation in COSMIC database
143 GTG del32 Val Fs. SM EG 1 798 Single report
195 ATC ACC Ile Thr SM F. P. 90 1011 Single report
194 CTT CGT Leu Arg SM G. C. 66 1011 Single report
306 CGA TGA Arg Stop SM G. M. 160 1011 Single report
282 CGG TGG Arg Trp SM GBM 600 1011 Single report
126 TAC TGC Tyr Cys SM IGROV-1 17 2249 wt in two other publications
270 TTT TTA Phe Leu DMD IGROV-1/Pt 7 606 Single report
282 CGG TGG Arg Trp DMD IGROV-1/Pt 600 606 Single report
281 GAC TAC Asp Tyr SM KURAMOCHI 16 144 Single report
126 TAC del21a Tyr InF SM NCI/ADR-RES 6 983 Single report
273 CGT CAT Arg His SM OC-314 780 2249 Mutation in COSMIC database
215 AGT CGT Ser Arg SM OV 90 4 1165 Single report
126 TAC TGC Tyr Cys SM OV1P 17 925 Single report
277 TGT TTT Cys Phe SM OVCA 432 48 1011 Single report
248 CGG CAG Arg Gln SM OVCAR-3 883 144 Single report
130 CTC GTC Leu Val SM OVCAR-4 22 2249 wt in another publication
224 GAG ins3 Glu InF SM OVCAR-5 1 864 wt in COSMIC
126 TAC del18 Tyr InF SM OVCAR-8 1 864 Single report
239 AAC GAC Asn Asp SM PA-1 53 854 Controversy with other publications. wt in COSMIC
316 CCC CCT Pro Pro SM PA-1 6 144 Controversy with other publications. wt in COSMIC
195 ATC ACC Ile Thr SM PM1015 90 798 Single report
275 TGT TAT Cys Tyr SM R. B. 87 1011 Single report
273 CGT CAT Arg His SM S. P. 780 1011 Single report
89 CCC del1a Pro Fs. SM SK-OV-3 3 2249 Controversy with other publications
179 CAT CGT His Arg SM SK-OV-3 146 1018 Controversy with other publications
262 GGT GTT Gly Val SM SW626 14 864 Controversy with other publications
273 CGT CAT Arg His SM SW626 780 1011 Controversy with other publications
175 CGC CAC Arg His SM TOV 112D 1187 1165 Single report
175 CGC CAC Arg His SM TYK-nu 1187 2249 Mutation in COSMIC database

 

 

 
 
Home | Our Work |p53 Info| p53 Database | p53 Link | Contact us