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

Pancreatic cancer

 

Table I : cell lines with wt p53

Cell line
ATCC
Reference
PK-45
1556

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
176 TGC AGC Cys Ser SM 8902 17 428 Single report
151 CCC TCC Pro Ser SM 8988S 92 428 Single report
134 TTT del1a Phe Fs. SM AsPC-1 4 397 Consensus based on four publications. Controversy with other publications
273 CGT CAT Arg His SM ASPC-1 780 132 Controversy with other publications. Excluded from the consensus
197 GTG TTG Val Leu SM BI 5 1653 Single report
275 TGT TAT Cys Tyr SM BJ 87 1653 Single report
220 TAT TGT Tyr Cys SM BxPC-3 336 176 Consensus based on six publications. A single publication decsribes a second mutation (neutral mutation)
159 GCC GTC Ala Val SM CAPAN-1 50 177 Confirmed in two other publications. wt in COSMIC
273 CGT CAT Arg His SM capan-2 780 132 wt in COSMIC
242 TGC CGC Cys Arg SM CFPAC-1 14 397 Single report
175 CGC CAC Arg His SM FAMPAC 1187 2116 Single report
272 GTG TTG Val Leu SM Ger 39 1653 Single report
262 GGT GTT Gly Val SM H-74 14 1689 Single report
151 CCC TCC Pro Ser SM HPAF-II 92 177 Confirmed in another publication
266 GGA GAA Gly Glu SM HPC-Y19 74 440 Single report
193 CAT CGT His Arg SM HPC-Y21 86 440 Single report
152 CCG del1a Pro Fs. SM HPC-YO 3 440 Single report
249 AGG ATG Arg Met SM Hs 700T 64 132 Confirmed in another publication
181 CGC CAC Arg His SM HS766T 34 132 Single report
282 CGG TGG Arg Trp SM HuP-T3 600 2249 Mutation in COSMIC database
255 ATC ACC Ile Thr SM HuP-T4 19 2249 Mutation in COSMIC database
130 CTC GTC Leu Val SM IMIM-PC-1 22 177 Single report
306 CGA TGA Arg Stop SM IMIM-PC-2 160 177 Single report
132 AAG AGG Lys Arg SM MCC1 51 2000 Single report
273 CGT TGT Arg Cys SM MDA-Panc3 687 1653 Single report
248 CGG TGG Arg Trp SM MIA PaCa-2 728 177 Confirmed in four other publications
209 AGA del2b Arg Fs. SM MZ1-PC 14 2249 Mutation in COSMIC database
282 CGG TGG Arg Trp SM MZ-PC-2 600 177 Single report
135 TGC TGG Cys Trp SM MZ-PC-4 25 177 Single report
282 CGG GGG Arg Gly SM PAN-03-JCK 48 1556 Single report
220 TAT TGT Tyr Cys SM Panc 89 336 176 Single report
273 CGT CAT Arg His SM Panc-1 780 178 Consensus based on four publications. Controversy with one publication
273 CGT TGT Arg Cys SM Panc-1 687 177 Controversy with other publications. Excluded from the cosnensus
255 ATC AAC Ile Asn SM PANC-10-05 6 2249 Mutation in COSMIC database
176 TGC AGC Cys Ser SM Panc-TU-I 17 176 Confirmed in another publication
175 CGC CAC Arg His SM PC 1187 1653 Single report
176 TGC AGC Cys Ser SM PC-44 17 428 Single report
237 ATG ATA Met Ile SM PCI-55 123 1556 Single report
237 ATG ATA Met Ile SM PK-1 123 1556 Single report
167 CAG TAG Gln Stop SM PK-8 40 1556 Single report
213 CGA TGA Arg Stop SM PK-9 306 1556 Single report
255 ATC ACC Ile Thr SM PL 45 19 965 Single report
132 AAG CAG Lys Gln SM PSN1 14 38 Single report
280 AGA AAA Arg Lys SM PT45 78 178 Single report
175 CGC CAC Arg His SM RWP-2 1187 177 Single report
282 CGG TGG Arg Trp SM SK-PC-1 600 177 Single report
179 CAT CGT His Arg SM SK-PC-3 146 177 Single report
175 CGC CAC Arg His SM SNU-213 1187 1491 Single report
238 TGT TAT Cys Tyr SM SNU-494 98 1491 Single report
245 GGC AGC Gly Ser SM SU86.86 440 397 Confirmed in another publication
273 CGT CAT Arg His SM Suit-2 780 1653 Single report
220 TAT TGT Tyr Cys SM T3M4 336 1653 Single report
273 CGT CAT Arg His SM UK Pan-1 780 659 Single report
179 CAT CGT His Arg SM YAPC 146 2249 Mutation in COSMIC database

 

 

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