long palpebral fissure Gene Set

Dataset	HPO Gene-Disease Associations
Category	disease or phenotype associations
Type	phenotype
Description	Distance between medial and lateral canthi is more than two standard deviations above the mean for age (objective); or, apparently increased length of the palpebral fissures. (Human Phenotype Ontology, HP_0000637)
External Link	http://compbio.charite.de/hpoweb/showterm?id=HP:0000637
Similar Terms
Downloads & Tools

Genes

16 genes associated with the long palpebral fissure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol	Name
ACTB	actin, beta
ACTG1	actin gamma 1
ANKRD11	ankyrin repeat domain 11
BMP1	bone morphogenetic protein 1
BRAF	B-Raf proto-oncogene, serine/threonine kinase
CLP1	cleavage and polyadenylation factor I subunit 1
KDM6A	lysine (K)-specific demethylase 6A
KMT2D	lysine (K)-specific methyltransferase 2D
KRAS	Kirsten rat sarcoma viral oncogene homolog
MAP2K1	mitogen-activated protein kinase kinase 1
MAP2K2	mitogen-activated protein kinase kinase 2
PIGO	phosphatidylinositol glycan anchor biosynthesis, class O
PIGV	phosphatidylinositol glycan anchor biosynthesis, class V
PIK3R2	phosphoinositide-3-kinase, regulatory subunit 2 (beta)
ROR2	receptor tyrosine kinase-like orphan receptor 2
WNT5A	wingless-type MMTV integration site family, member 5A