TP63, tumor protein p63, 8626

N. diseases: 816; N. variants: 64
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0000846
Disease: Agenesis
Agenesis
0.020 GeneticVariation disease BEFREE Vomer aplasia in a patient carrying a de novo mutation of the TP63 gene (3q27). 23906991 2013
CUI: C0000846
Disease: Agenesis
Agenesis
0.020 Biomarker disease BEFREE Msx1, Pax9, and Axin2 are involved in non-syndromic hypodontia, while genes such as Shh, Pitx2, Irf6, and p63 are considered to participate in syndromic genetic disorders, which include tooth agenesis. 18573979 2008