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TP63

tumor protein p63

HCNC Approved Symbol
TP63 (HGNC:15979)
Genomic Coordinates
3:189,596,746 - 189,897,276 (3q28)
Synonyms
p51, SHFM4, EEC3, p63, p73L, OFC8, KET, p73H, NBP, p53CP, p40, TP73L, TP53L, TP53CP
Disease Associations
This gene is associated with the following 8 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
ADULT syndrome
103285AD
Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3
604292AD
Hay-Wells syndrome
106260AD
Limb-mammary syndrome
603543AD
Orofacial cleft 8
618149-
Premature ovarian failure 21
620311AD
Rapp-Hodgkin syndrome
129400AD
Split-hand/foot malformation 4
605289AD

Diagnosed Cases

13Patients

In total, 13 patients were diagnosed with a variant in the TP63 gene.

Frequently observed phenotypes

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

Foot ectrodactyly
 4 (30.8%)
Syndactyly
 2 (15.4%)
Hand ectrodactyly
 2 (15.4%)
Split hand
 2 (15.4%)
Cleft palate
 2 (15.4%)