TP53 gene homepage

General information
Gene symbol TP53
Gene name tumor protein p53
Chromosome 17
Chromosomal band p13.1
Imprinted Unknown
Genomic reference LRG_321
Transcript reference NM_000546.5, NM_001126112.2, NM_001126113.2, NM_001126114.2, NM_001126115.1, NM_001126116.1, NM_001126117.1, NM_001126118.1, NM_001276695.1, NM_001276696.1, NM_001276697.1, NM_001276698.1, NM_001276699.1, NM_001276760.1, NM_001276761.1
Associated with diseases ADCC, BCC7, BMFS5, BrCa, CPP, CRC, GLM1, LFS, OSRC
Citation reference(s) -
Curators (1) Despoina Kalfakakou
Total number of public variants reported 210
Unique public DNA variants reported 48
Individuals with public variants 252
Hidden variants 0
Date created May 20, 2020
Date last updated May 16, 2022
Version TP53:220516

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
HGNC 11998
Entrez Gene 7157
PubMed articles TP53
OMIM - Gene 191170
OMIM - Diseases ADCC (Adrenocortical carcinoma, pediatric)
BCC7 (Basal cell carcinoma 7)
BMFS5 (Bone marrow failure syndrome 5)
BrCa (Breast Cancer)
CPP (Choroid plexus papilloma)
CRC (Colorectal cancer)
GLM1 (Glioma susceptibility 1)
LFS (Li-Fraumeni syndrome)
OSRC (Osteosarcoma)


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00000213 17 transcript variant 1 NM_000546.5 NP_000537.3 210
00000214 17 transcript variant 1 NM_001276760.1 NP_001263689.1 210
00000215 17 transcript variant 2 NM_001126112.2 NP_001119584.1 210
00000216 17 transcript variant 2 NM_001276761.1 NP_001263690.1 210
00000217 17 transcript variant 3 NM_001126114.2 NP_001119586.1 210
00000218 17 transcript variant 3 NM_001276696.1 NP_001263625.1 210
00000219 17 transcript variant 4 NM_001126113.2 NP_001119585.1 210
00000220 17 transcript variant 4 NM_001276695.1 NP_001263624.1 210
00000221 17 transcript variant 5 NM_001126115.1 NP_001119587.1 210
00000222 17 transcript variant 5 NM_001276697.1 NP_001263626.1 210
00000223 17 transcript variant 6 NM_001126116.1 NP_001119588.1 210
00000224 17 transcript variant 6 NM_001276698.1 NP_001263627.1 210
00000225 17 transcript variant 7 NM_001126117.1 NP_001119589.1 210
00000226 17 transcript variant 7 NM_001276699.1 NP_001263628.1 210
00000227 17 transcript variant 8 NM_001126118.1 NP_001119590.1 210


Copyright & disclaimer
The contents of this LOVD database are the intellectual property of the respective curator(s). Any unauthorised use, copying, storage or distribution of this material without written permission from the curator(s) will lead to copyright infringement with possible ensuing litigation. Copyright © 2020-2024. All Rights Reserved. For further details, refer to Directive 96/9/EC of the European Parliament and the Council of March 11 (1996) on the legal protection of databases.

We have used all reasonable efforts to ensure that the information displayed on these pages and contained in the databases is of high quality. We make no warranty, express or implied, as to its accuracy or that the information is fit for a particular purpose, and will not be held responsible for any consequences arising out of any inaccuracies or omissions. Individuals, organisations and companies which use this database do so on the understanding that no liability whatsoever either direct or indirect shall rest upon the curator(s) or any of their employees or agents for the effects of any product, process or method that may be produced or adopted by any part, notwithstanding that the formulation of such product, process or method may be based upon information here provided.