cheilitis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A lip disease characterized by the inflammation of the lips; which may include the perioral skin, the vermilion border and the labial mucosa. (Human Disease Ontology, DOID_1762)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0100825
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Genes

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

Symbol Name
CARD9 caspase recruitment domain family, member 9
CLEC7A C-type lectin domain family 7, member A
COL7A1 collagen, type VII, alpha 1
FERMT1 fermitin family member 1
HLCS holocarboxylase synthetase (biotin-(proprionyl-CoA-carboxylase (ATP-hydrolysing)) ligase)
IL17F interleukin 17F
IL17RA interleukin 17 receptor A
MBTPS2 membrane-bound transcription factor peptidase, site 2
OCRL oculocerebrorenal syndrome of Lowe
SLC39A4 solute carrier family 39 (zinc transporter), member 4
SLC46A1 solute carrier family 46 (folate transporter), member 1
STAT1 signal transducer and activator of transcription 1, 91kDa
TRAF3IP2 TRAF3 interacting protein 2