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

Esophageal cancer

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)

Esophageal adenocarcinoma

Pos.
WT
Mut
      AA
Mut
Comp
Name
NB
Ref
Comments
273 CGT AGT Arg Ser DMU Bic-1 20 2004 Single report
309 CCC TCC Pro Ser DMU Bic-1 6 2004 Single report
277 TGT TTT Cys Phe SM Flo-1 48 2004 Single report
310 AAC ins1a Asn Fs. SM OE19 1 2249 Mutation in COSMIC database

Esophageal SCC

Pos.
WT
Mut
      AA
Mut
Comp
Name
NB
Ref
Comments
248 CGG TGG Arg Trp SM COLO-680N 728 2249 Mutation in COSMIC database
234 TAC TGC Tyr Cys SM EC-GI-10 133 2249 Mutation in COSMIC database
245 GGC GTC Gly Val SM HCE-4 84 5 wt in COSMIC
278 CCT TCT Pro Ser SM HCE-6 87 5 Single report
278 CCT TCT Pro Ser SM HCE7 87 1317 Single report
220 TAT TGT Tyr Cys SM KYSE- 890 336 634 Single report
337 CGC TGC Arg Cys SM KYSE-110 19 634 Single report
193 CAT CTT His Leu DMU KYSE-1170 55 634 Single report
255 ATC GTC Ile Val DMU KYSE-1170 4 634 Single report
194 CTT GTT Leu Val SM KYSE-1240 3 634 Single report
193 CAT CTT His Leu SM KYSE-1250 55 634 Single report
342 CGA del7a Arg Fs. SM KYSE-1260 1 634 Single report
193 CAT CGT His Arg SM KYSE-140 86 634 Single report
248 CGG CAG Arg Gln SM KYSE-150 883 2249 Mutation in COSMIC database
266 GGA CGA Gly Arg SM KYSE-170 20 634 Single report
195 ATC ACC Ile Thr SM KYSE-180 90 2249 Mutation in COSMIC database
203 GTG CTG Val Leu SM KYSE-190 2 634 Single report
337 CGC TGC Arg Cys SM KYSE-200 19 634 Single report
248 CGG TGG Arg Trp SM KYSE-220 728 634 Single report
248 CGG CAG Arg Gln SM KYSE-350 883 634 Single report
337 CGC TGC Arg Cys SM KYSE-410 19 2249 Mutation in COSMIC database
179 CAT CGT His Arg SM KYSE-450 146 634 Controversy with other publications
339 GAG TAG Glu Stop SM KYSE-450 12 2249 Controversy with other publications
241 TCC del32c Ser Fs. SM KYSE-510 1 634 Controversy with other publications
343 GAG TAG Glu Stop SM KYSE-510 5 2249 Controversy with other publications
266 GGA CGA Gly Arg SM KYSE-590 20 634 Single report
251 ATC ins1a Ile Fs. SM KYSE-70 1 634 Single report
273 CGT TGT Arg Cys SM KYSE-850 687 634 Single report
175 CGC CAC Arg His SM SK-GT-4 1187 462 Single report
214 CAT CGT His Arg SM T.T 69 1006 Single report
272 GTG ATG Val Met SM T.Tn 105 1006 Single report
272 GTG ATG Val Met SM TE-1 105 1144 wt in COSMIC
242 TGC TAC Cys Tyr SM TE-10 58 1144 Single report
110 CGT CTT Arg Leu SM TE-11 28 1006 Controversy with other publications. wt in COSMIC
237 ATG ATT Met Ile SM TE-11 52 1144 Controversy with other publications. wt in COSMIC
342 CGA TGA Arg Stop SM TE-15 74 2249 Mutation in COSMIC database
248 CGG CAG Arg Gln SM TE-6 883 1144 Single report
237 ATG ATT Met Ile SM TE-8 52 2249 Mutation in COSMIC database
267 CGG del1b Arg Fs. SM TE-9 2 1144 wt in COSMIC

 

 

 

 
 
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