parakeratosis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Abnormal formation of the keratinocytes of the epidermis characterized by persistence of nuclei, incomplete formation of keratin, and moistness and swelling of the keratinocytes. (Human Phenotype Ontology, HP_0001036)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001036
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Genes

10 genes associated with the parakeratosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CLDN1 claudin 1
CYP4F22 cytochrome P450, family 4, subfamily F, polypeptide 22
IL36RN interleukin 36 receptor antagonist
MBTPS2 membrane-bound transcription factor peptidase, site 2
NIPAL4 NIPA-like domain containing 4
NLRP1 NLR family, pyrin domain containing 1
NSDHL NAD(P) dependent steroid dehydrogenase-like
POMP proteasome maturation protein
RHBDF2 rhomboid 5 homolog 2 (Drosophila)
TRPV3 transient receptor potential cation channel, subfamily V, member 3