Peeling skin syndrome

Gene: TP63

Red List (low evidence)

TP63 (tumor protein p63)
EnsemblGeneIds (GRCh38): ENSG00000073282
EnsemblGeneIds (GRCh37): ENSG00000073282
OMIM: 603273, Gene2Phenotype
TP63 is in 14 panels

1 review

David Kelsell (Queen Mary University of London)

Red List (low evidence)

Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown

Phenotypes
Hay-Wells syndrome, 106260; Red, cracking, peeling skin at birth

History Filter Activity

12 Dec 2016, Gel status: 0

panel promoted to version 1

Rebecca Foulger (Genomics England curator)

12 December 2016: Reviews were assessed, and panel was revised according to expert review and additional curation.

8 Dec 2016, Gel status: 0

Created

Rebecca Foulger (Genomics England curator)

TP63 was created by rfoulger

8 Dec 2016, Gel status: 0

Added New Source

Rebecca Foulger (Genomics England curator)

TP63 was added to Peeling skin syndromepanel. Sources: Other