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
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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