abnormality of the lacrimal duct Gene Set

Dataset	HPO Gene-Disease Associations
Category	disease or phenotype associations
Type	phenotype
Description	An abnormality of the lacrimal duct, a duct that drain tears from the conjunctiva, via the lacrimal puncta, into the lacrimal sac. (Human Phenotype Ontology, HP_0011481)
External Link	http://compbio.charite.de/hpoweb/showterm?id=HP:0011481
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Genes

16 genes associated with the abnormality of the lacrimal duct phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol	Name
CD151	CD151 molecule (Raph blood group)
CREBBP	CREB binding protein
EYA1	EYA transcriptional coactivator and phosphatase 1
FGF10	fibroblast growth factor 10
FGFR2	fibroblast growth factor receptor 2
FGFR3	fibroblast growth factor receptor 3
FRAS1	Fraser extracellular matrix complex subunit 1
FREM1	FRAS1 related extracellular matrix 1
FREM2	FRAS1 related extracellular matrix protein 2
GRIP1	glutamate receptor interacting protein 1
NOP10	NOP10 ribonucleoprotein
PAX1	paired box 1
PTDSS1	phosphatidylserine synthase 1
TCOF1	Treacher Collins-Franceschetti syndrome 1
TFAP2A	transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)
TP63	tumor protein p63