plantar hyperkeratosis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Hyperkeratosis affecting the sole of the foot. (Human Phenotype Ontology, HP_0007556)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0007556
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Genes

28 genes associated with the plantar hyperkeratosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AAAS achalasia, adrenocortical insufficiency, alacrimia
COG6 component of oligomeric golgi complex 6
COL17A1 collagen, type XVII, alpha 1
CTSC cathepsin C
DSP desmoplakin
FERMT1 fermitin family member 1
GJB2 gap junction protein, beta 2, 26kDa
GJB6 gap junction protein, beta 6, 30kDa
HPGD hydroxyprostaglandin dehydrogenase 15-(NAD)
ITGB4 integrin, beta 4
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
KRT9 keratin 9, type I
LAMA3 laminin, alpha 3
LAMB3 laminin, beta 3
LAMC2 laminin, gamma 2
MBTPS2 membrane-bound transcription factor peptidase, site 2
PIGL phosphatidylinositol glycan anchor biosynthesis, class L
PLEC plectin
PTEN phosphatase and tensin homolog
PVRL1 poliovirus receptor-related 1 (herpesvirus entry mediator C)
RHBDF2 rhomboid 5 homolog 2 (Drosophila)
SLURP1 secreted LY6/PLAUR domain containing 1
WNT10A wingless-type MMTV integration site family, member 10A