ectropion Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000656
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Genes

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

Symbol Name
ABCA1 ATP-binding cassette, sub-family A (ABC1), member 1
ABCA12 ATP-binding cassette, sub-family A (ABC1), member 12
ABHD5 abhydrolase domain containing 5
ALOX12B arachidonate 12-lipoxygenase, 12R type
DDB2 damage-specific DNA binding protein 2, 48kDa
DHODH dihydroorotate dehydrogenase (quinone)
ERCC2 excision repair cross-complementation group 2
ERCC6 excision repair cross-complementation group 6
ITGA6 integrin, alpha 6
ITGB4 integrin, beta 4
KDM6A lysine (K)-specific demethylase 6A
KMT2D lysine (K)-specific methyltransferase 2D
MBTPS2 membrane-bound transcription factor peptidase, site 2
NIPAL4 NIPA-like domain containing 4
POLH polymerase (DNA directed), eta
SAT1 spermidine/spermine N1-acetyltransferase 1
TGM1 transglutaminase 1
XPA xeroderma pigmentosum, complementation group A
XPC xeroderma pigmentosum, complementation group C