TP63, tumor protein p63, 8626

N. diseases: 816; N. variants: 64
Disease: Rudiger syndrome 1 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0406704
Disease: Rudiger syndrome 1
Rudiger syndrome 1 		0.800 Biomarker disease MGD p63 is a p53 homologue required for limb and epidermal morphogenesis. 10227293 1999
CUI: C0406704
Disease: Rudiger syndrome 1
Rudiger syndrome 1 		0.800 Biomarker disease MGD p63 is essential for regenerative proliferation in limb, craniofacial and epithelial development. 10227294 1999
CUI: C0406704
Disease: Rudiger syndrome 1
Rudiger syndrome 1 		0.800 GeneticVariation disease BEFREE Transactivation studies with these mutant p63 isotypes provide a molecular explanation for the dominant character of p63 mutations in EEC syndrome. 10535733 1999
CUI: C0406704
Disease: Rudiger syndrome 1
Rudiger syndrome 1 		0.800 GeneticVariation disease BEFREE The two amino acids mutated in the families with SHFM appear to be primarily involved in maintenance of the overall structure of the domain, in contrast to the p63 mutations responsible for EEC syndrome, which reside in amino acid residues that directly interact with the DNA. 10839977 2000
CUI: C0406704
Disease: Rudiger syndrome 1
Rudiger syndrome 1 		0.800 GeneticVariation disease BEFREE As with most other p63 mutations in EEC syndrome, this mutation has arisen de novo and is located within the core DNA-binding domain of p63. 11012604 2000
CUI: C0406704
Disease: Rudiger syndrome 1
Rudiger syndrome 1 		0.800 Biomarker disease MGD p63 is a prostate basal cell marker and is required for prostate development. 11106548 2000
CUI: C0406704
Disease: Rudiger syndrome 1
Rudiger syndrome 1 		0.800 GeneticVariation disease BEFREE We have recently demonstrated that heterozygous mutations in the p63 gene are the major cause of EEC syndrome. 11159940 2001
CUI: C0406704
Disease: Rudiger syndrome 1
Rudiger syndrome 1 		0.800 Biomarker disease CTD_human The results differed for these three conditions. p63 gene mutations were detected in almost all (40/43) individuals affected with EEC syndrome. 11462173 2001
CUI: C0406704
Disease: Rudiger syndrome 1
Rudiger syndrome 1 		0.800 GeneticVariation disease BEFREE The results differed for these three conditions. p63 gene mutations were detected in almost all (40/43) individuals affected with EEC syndrome. 11462173 2001
CUI: C0406704
Disease: Rudiger syndrome 1
Rudiger syndrome 1 		0.800 GeneticVariation disease BEFREE Germline mis-sense mutations in the DNA-binding domain of the p63 gene have recently been established as the molecular basis for the autosomal dominant EEC (Ectrodactyly, Ectodermal dysplasia, Clefting) syndrome. 11903230 2002
CUI: C0406704
Disease: Rudiger syndrome 1
Rudiger syndrome 1 		0.800 GeneticVariation disease BEFREE Mutations in the p63 gene are found in a number of human syndromes, including ectrodactyly-ectodermal dysplasia-cleft lip/palate (EEC) syndrome, limb-mammary syndrome (LMS), Hay-Wells syndrome and in non-syndromic split-hand/split-foot malformation (SHFM). 11929852 2002
CUI: C0406704
Disease: Rudiger syndrome 1
Rudiger syndrome 1 		0.800 GeneticVariation disease BEFREE We identified heterozygous p63 mutations in three unrelated cases of EEC syndrome, two Iowa white families and one sporadic case in a Filipino boy. 12161593 2002
CUI: C0406704
Disease: Rudiger syndrome 1
Rudiger syndrome 1 		0.800 Biomarker disease MGD p63 Coordinates anogenital modeling and epithelial cell differentiation in the developing female urogenital tract. 12368184 2002
CUI: C0406704
Disease: Rudiger syndrome 1
Rudiger syndrome 1 		0.800 Biomarker disease MGD Loss of p63 expression is associated with tumor progression in bladder cancer. 12368193 2002
CUI: C0406704
Disease: Rudiger syndrome 1
Rudiger syndrome 1 		0.800 GeneticVariation disease BEFREE TP63 mutation and clefting modifier genes in an EEC syndrome family. 15324320 2004
CUI: C0406704
Disease: Rudiger syndrome 1
Rudiger syndrome 1 		0.800 GeneticVariation disease BEFREE This report expands the knowledge of genotype-phenotype data on the p63 gene and suggests there may be a considerable overlap between the EEC syndrome and the ADULT syndrome. 17041931 2006
CUI: C0406704
Disease: Rudiger syndrome 1
Rudiger syndrome 1 		0.800 Biomarker disease MGD DeltaNp63 plays an anti-apoptotic role in ventral bladder development. 17079275 2006
CUI: C0406704
Disease: Rudiger syndrome 1
Rudiger syndrome 1 		0.800 GeneticVariation disease BEFREE Of the six cases/families now reported with EEC syndrome and Arg227Gln TP63 mutation, four have manifested this distinct urological abnormality, indicative of a genotype-phenotype correlation. 17431922 2007
CUI: C0406704
Disease: Rudiger syndrome 1
Rudiger syndrome 1 		0.800 GeneticVariation disease BEFREE Mutations in the p63 gene have been identified in five types of syndromic ectodermal dysplasias (EDs) with overlapping phenotypes: Ectrodactyly-Ectodermal dysplasia-Clefting (EEC syndrome, MIM 604292), Ankyloblepharon-Ectodermal dysplasia-Clefting (AEC syndrome, MIM 106260) [3], Acro-Dermato-Ungueal-Lacrimal-Tooth (ADULT syndrome, MIM 103285), Rapp-Hodgkin (RHS syndrome, MIM 129400) and Limb-Mammary (LMS syndrome, MIM 603543) [2]. 18603493 2008
CUI: C0406704
Disease: Rudiger syndrome 1
Rudiger syndrome 1 		0.800 GeneticVariation disease BEFREE The TP63 gene molecular study showed in both siblings a heterozygous H208D mutation, which has not been previously reported to our knowledge, suggesting that this molecular lesion is associated with EEC syndrome without orofacial clefting. 19663851 2009
CUI: C0406704
Disease: Rudiger syndrome 1
Rudiger syndrome 1 		0.800 GeneticVariation disease BEFREE Pathogenic mutations in the TP63 transcription factor have been identified as the molecular basis of EEC syndrome and to date 34 mutations have been reported. 19903181 2010
CUI: C0406704
Disease: Rudiger syndrome 1
Rudiger syndrome 1 		0.800 GeneticVariation disease BEFREE In this paper we describe a 17-year-old girl affected by ectrodactyly-ectodermal dysplasia-clefting syndrome with a de novo p63 mutation that predicts a heterozygous missense substitution (arginine to tryptophan substitution caused by a cytosine to thymine transition) at the amino acid 304 (R304W) of the p63 DNA-binding domain. 20180707 2010
CUI: C0406704
Disease: Rudiger syndrome 1
Rudiger syndrome 1 		0.800 GeneticVariation disease BEFREE Here, we characterize the transcriptional activity and protein stability of ΔNp63 mutants (that is, mutants of a p63 isoform that lacks the N-terminal transactivation domain) that are found in ectrodactyly-ectodermal dysplasia-cleft syndrome (EEC), ankyloblepharon-ectodermal dysplasia-clefting syndrome (AEC) and nonsyndromic split-hand/split-foot malformation (SHFM). 21652629 2011
CUI: C0406704
Disease: Rudiger syndrome 1
Rudiger syndrome 1 		0.800 Biomarker disease MGD Residual embryonic cells as precursors of a Barrett's-like metaplasia. 21703447 2011
CUI: C0406704
Disease: Rudiger syndrome 1
Rudiger syndrome 1 		0.800 GeneticVariation disease BEFREE Heterozygous p63 mutations cause the EEC syndrome and result in visual impairment owing to progressive LSCD. 21959367 2012