wrinkled skin Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description The presence of an increased degree of wrinkling (irregular folds and indentations) of the skin as compared with age-related norms. (Human Phenotype Ontology, HP_0100678)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001211
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22 gene mutations causing the wrinkled skin phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ASPRV1 aspartic peptidase, retroviral-like 1
ASS1 argininosuccinate synthase 1
C8ORF44-SGK3 C8orf44-SGK3 readthrough
CASK calcium/calmodulin-dependent serine protein kinase (MAGUK family)
CBS cystathionine-beta-synthase
CLDN1 claudin 1
CLDN7 claudin 7
DSG4 desmoglein 4
EN1 engrailed homeobox 1
FOXN1 forkhead box N1
GBA glucosidase, beta, acid
HR hair growth associated
KCNJ1 potassium channel, inwardly rectifying subfamily J, member 1
MYBL1 v-myb avian myeloblastosis viral oncogene homolog-like 1
OTC ornithine carbamoyltransferase
PLAGL1 pleiomorphic adenoma gene-like 1
SCD stearoyl-CoA desaturase (delta-9-desaturase)
SP6 Sp6 transcription factor
ST14 suppression of tumorigenicity 14 (colon carcinoma)
TGM1 transglutaminase 1
TP63 tumor protein p63
ZDHHC13 zinc finger, DHHC-type containing 13