palmoplantar keratosis Gene Set

Dataset DISEASES Curated Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A keratosis characterized by abnormal thickening of the palms and the soles. (Human Disease Ontology, DOID_3390)
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Genes

29 genes involed in the disease palmoplantar keratosis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
AAGAB alpha- and gamma-adaptin binding protein
AQP5 aquaporin 5
CTSC cathepsin C
DSG1 desmoglein 1
DSP desmoplakin
GJB2 gap junction protein, beta 2, 26kDa
GJB3 gap junction protein, beta 3, 31kDa
GJB4 gap junction protein, beta 4, 30.3kDa
GJB6 gap junction protein, beta 6, 30kDa
JUP junction plakoglobin
KRT1 keratin 1, type II
KRT14 keratin 14, type I
KRT16 keratin 16, type I
KRT17 keratin 17, type I
KRT6A keratin 6A, type II
KRT6B keratin 6B, type II
KRT6C keratin 6C, type II
KRT9 keratin 9, type I
LOR loricrin
MBTPS2 membrane-bound transcription factor peptidase, site 2
POMP proteasome maturation protein
RHBDF2 rhomboid 5 homolog 2 (Drosophila)
RSPO1 R-spondin 1
SERPINB7 serpin peptidase inhibitor, clade B (ovalbumin), member 7
SLURP1 secreted LY6/PLAUR domain containing 1
SNAP29 synaptosomal-associated protein, 29kDa
TAT tyrosine aminotransferase
TRPV3 transient receptor potential cation channel, subfamily V, member 3
WNT10A wingless-type MMTV integration site family, member 10A