pustule Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A small elevation of the skin containing cloudy or purulent material usually consisting of necrotic inflammatory cells. (Human Phenotype Ontology, HP_0200039)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0200039
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Genes

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

Symbol Name
ADAM17 ADAM metallopeptidase domain 17
CARD14 caspase recruitment domain family, member 14
CTSC cathepsin C
ECM1 extracellular matrix protein 1
FERMT1 fermitin family member 1
IL36RN interleukin 36 receptor antagonist
LPIN2 lipin 2
PSTPIP1 proline-serine-threonine phosphatase interacting protein 1
SLC39A4 solute carrier family 39 (zinc transporter), member 4
TMC6 transmembrane channel-like 6
TMC8 transmembrane channel-like 8