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Gene entry

TP63

tumor protein p63

Chromosome
3
Cytoband
3q28
Variants (rsID)
115

TP63 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 3 (region 3q28). Its official name is “tumor protein p63”. The reference table lists 115 variants (rsID) for this gene.

Clinically classified variants

10 reference-table entries with clinical significance.

  • rs148076109Benignsingle nucleotide variantEctrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3|TP63-Related Spectrum Disorders|Orofacial cleft 8
  • rs34875865Benignsingle nucleotide variant
  • rs9840360Benignsingle nucleotide variant
  • rs113993967Pathogenicsingle nucleotide variantADULT syndrome|TP63-Related Spectrum Disorders
  • rs121908835Pathogenicsingle nucleotide variantEctrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3|TP63-Related Spectrum Disorders|Rapp-Hodgkin ectodermal dysplasia syndrome
  • rs121908840Pathogenicsingle nucleotide variantRapp-Hodgkin ectodermal dysplasia syndrome|Ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3|TP63-Related Spectrum Disorders
  • rs121908841Pathogenicsingle nucleotide variantEctrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3|TP63-Related Spectrum Disorders|Inborn genetic diseases
  • rs121908844Pathogenicsingle nucleotide variantEctrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3
  • rs121908849Pathogenicsingle nucleotide variantEctrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3|ADULT syndrome|TP63-Related Spectrum Disorders
  • rs864621968Pathogenicsingle nucleotide variantEctrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3|TP63-Related Spectrum Disorders

Other listed variants

Public references

Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.