A·TC·GC·GA·TC·GG·CT·AG·CA·TT·A
Xysera Locus
SourcesHuman / GRCh38
Gene/Homo sapiens

TP53

tumor protein p53

17p13.1chr17:7,661,779–7,687,546- strandGRCh38
Record assembledPartial sources
Type
Protein Coding
Chromosome
chr17
NCBI Gene ID
7157
Ensembl Gene ID
ENSG00000141510
Aliases
BCC7 · BMFS5 · LFS1 · P53 · TRP53
Chromosome locatorchr17
TP53
pter · 0 Mb17p13.183 Mb · qter
Partial recordPhenotype associations are temporarily unavailable.
01/

Gene structure

Source / Ensembl · GRCh38
11exons
25,768genomic bp
Viewing transcriptTP53-201
Transcript context40 isoforms
Displayed isoform
protein coding1,182 bp CDS
3′5′Exon 1: 7,668,421–7,669,690 (1,270 bp)EXON 17,668,421–7,669,690 · 1,270 bpExon 2: 7,670,609–7,670,715 (107 bp)EXON 27,670,609–7,670,715 · 107 bpExon 3: 7,673,535–7,673,608 (74 bp)EXON 37,673,535–7,673,608 · 74 bpExon 4: 7,673,701–7,673,837 (137 bp)EXON 47,673,701–7,673,837 · 137 bpExon 5: 7,674,181–7,674,290 (110 bp)EXON 57,674,181–7,674,290 · 110 bpExon 6: 7,674,859–7,674,971 (113 bp)EXON 67,674,859–7,674,971 · 113 bpExon 7: 7,675,053–7,675,236 (184 bp)EXON 77,675,053–7,675,236 · 184 bpExon 8: 7,675,994–7,676,272 (279 bp)EXON 87,675,994–7,676,272 · 279 bpExon 9: 7,676,382–7,676,403 (22 bp)EXON 97,676,382–7,676,403 · 22 bpExon 10: 7,676,521–7,676,622 (102 bp)EXON 107,676,521–7,676,622 · 102 bpExon 11: 7,687,377–7,687,490 (114 bp)EXON 117,687,377–7,687,490 · 114 bp7,668,4217,673,1887,677,9567,682,7237,687,490
Select an exon

Click an exon block to inspect its genomic coordinates and length.

CDS UTR / non-coding exon Intron · Proportional genomic coordinates

02/

Function

Source / NCBI Gene

This gene encodes a tumor suppressor protein containing transcriptional activation, DNA binding, and oligomerization domains. The encoded protein responds to diverse cellular stresses to regulate expression of target genes, thereby inducing cell cycle arrest, apoptosis, senescence, DNA repair, or changes in metabolism. Mutations in this gene are associated with a variety of human cancers, including hereditary cancers such as Li-Fraumeni syndrome. Alternative splicing of this gene and the use of alternate promoters result in multiple transcript variants and isoforms. Additional isoforms have also been shown to result from the use of alternate translation initiation codons from identical transcript variants (PMIDs: 12032546, 20937277). [provided by RefSeq, Dec 2016]

03/

Protein

Source / UniProtKB · Reviewed

Recommended name

Cellular tumor antigen p53

Accession
P04637
Length
393 aa
Status
Reviewed
Functional annotations16 curated statements
  1. 01

    Multifunctional transcription factor that induces cell cycle arrest, DNA repair or apoptosis upon binding to its target DNA sequence.

  2. 02

    Acts as a tumor suppressor in many tumor types; induces growth arrest or apoptosis depending on the physiological circumstances and cell type.

  3. 03

    Negatively regulates cell division by controlling expression of a set of genes required for this process.

  4. 04

    One of the activated genes is an inhibitor of cyclin-dependent kinases.

  5. 05

    Apoptosis induction seems to be mediated either by stimulation of BAX and FAS antigen expression, or by repression of Bcl-2 expression.

SourcesUniProtKB / P04637 ↗
Referenced literature

PMID 11025664 ↗PMID 12524540 ↗PMID 12810724 ↗PMID 15186775 ↗PMID 15340061 ↗PMID 17317671 ↗PMID 17349958 ↗PMID 19556538 ↗PMID 20673990 ↗PMID 20959462 ↗PMID 22726440 ↗PMID 24051492 ↗PMID 24652652 ↗PMID 35618207 ↗PMID 36634798 ↗PMID 38653238 ↗PMID 9840937 ↗PMID 17189187 ↗

04/

Expression

Source / Human Protein Atlas
Top 10 consensus tissues
RNA expression · nTPM

Hover a bar for its exact value. Linear scale preserves proportional differences. · HPA consensus tissue dataset.

05/

Associated conditions

Source / Ensembl Phenotypes
No phenotype associations were returned by the source.

Associations are reproduced from the named sources and do not independently establish causality. Not for clinical interpretation.

06/

Literature

Source / PubMed
  1. 2023
    The Role of TP53 in Adaptation and Evolution.

    Voskarides K, Giannopoulou N

    Cells · PMID 36766853

    ↗
  2. 2010
    TP53 mutations in human cancers: origins, consequences, and clinical use.

    Olivier M, Hollstein M, Hainaut P

    Cold Spring Harbor perspectives in biology · PMID 20182602

    ↗
  3. 2016
    TP53 Variations in Human Cancers: New Lessons from the IARC TP53 Database and Genomics Data.

    Bouaoun L, Sonkin D, Ardin M, Hollstein M, Byrnes G, et al.

    Human mutation · PMID 27328919

    ↗
  4. 2011
    TP53 mutations in nonsmall cell lung cancer.

    Mogi A, Kuwano H

    Journal of biomedicine & biotechnology · PMID 21331359

    ↗
  5. 2020
    Li-Fraumeni syndrome heterogeneity.

    Gargallo P, Yáñez Y, Segura V, Juan A, Torres B, et al.

    Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · PMID 31691207

    ↗
07/

Sources & identifiers

Identity · function · literatureNCBIGene 7157Coordinates · transcript · phenotypeEnsemblENSG00000141510Protein annotationUniProtKBP04637Research literaturePubMed5 selected records
Xysera Locus

Research and educational information only. Not medical advice.

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