Palmoplantar Keratosis Gene Set

Dataset DisGeNET Gene-Disease Associations
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)
External Link https://www.disgenet.org/browser/0/1/0/C0022596
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Genes

39 genes associated with the disease Palmoplantar Keratosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
AAAS achalasia, adrenocortical insufficiency, alacrimia
AKT1 v-akt murine thymoma viral oncogene homolog 1
COG6 component of oligomeric golgi complex 6
CTSC cathepsin C
DKC1 dyskeratosis congenita 1, dyskerin
DSG1 desmoglein 1
DSP desmoplakin
FERMT1 fermitin family member 1
GJA1 gap junction protein, alpha 1, 43kDa
GJB2 gap junction protein, beta 2, 26kDa
GJB6 gap junction protein, beta 6, 30kDa
HPGD hydroxyprostaglandin dehydrogenase 15-(NAD)
HRAS Harvey rat sarcoma viral oncogene homolog
KDSR 3-ketodihydrosphingosine reductase
KRT1 keratin 1, type II
KRT10 keratin 10, type I
KRT14 keratin 14, type I
KRT16 keratin 16, type I
KRT17 keratin 17, type I
KRT5 keratin 5, type II
KRT6A keratin 6A, type II
KRT83 keratin 83, type II
KRT9 keratin 9, type I
MBTPS2 membrane-bound transcription factor peptidase, site 2
NECTIN1 nectin cell adhesion molecule 1
PIGL phosphatidylinositol glycan anchor biosynthesis, class L
PIK3CA phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit alpha
PKP1 plakophilin 1
PLEC plectin
PTEN phosphatase and tensin homolog
RARA retinoic acid receptor, alpha
RSPO1 R-spondin 1
SDR9C7 short chain dehydrogenase/reductase family 9C, member 7
SERPINB7 serpin peptidase inhibitor, clade B (ovalbumin), member 7
SLURP1 secreted LY6/PLAUR domain containing 1
SNAP29 synaptosomal-associated protein, 29kDa
TAT tyrosine aminotransferase
TERT telomerase reverse transcriptase
TGM1 transglutaminase 1