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PERP

p53 apoptosis effector related to PMP22

HCNC Approved Symbol
PERP (HGNC:17637)
Genomic Coordinates
6:138,088,505 - 138,107,419 (6q23.3)
Synonyms
PIGPC1, dJ496H19.1, KCP1, THW, KRTCAP1
Disease Associations
This gene is associated with the following 2 diseases in OMIM.

Diagnosed Cases

1Patient

In total, 1 patient was diagnosed with a variant in the PERP gene.

Frequently observed phenotypes

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

Lymphadenopathy
 1 (100.0%)
Onychomycosis
 1 (100.0%)
Recurrent skin infections
 1 (100.0%)
PERP - Gene browser | 3billion