septo-optic dysplasia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Underdevelopment of the optic nerve and absence of the septum pellucidum. (Human Phenotype Ontology, HP_0100842)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0100842
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Genes

11 genes associated with the septo-optic dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
FGFR1 fibroblast growth factor receptor 1
HESX1 HESX homeobox 1
LHX3 LIM homeobox 3
LHX4 LIM homeobox 4
OTX2 orthodenticle homeobox 2
POU1F1 POU class 1 homeobox 1
PROKR2 prokineticin receptor 2
PROP1 PROP paired-like homeobox 1
SOX2 SRY (sex determining region Y)-box 2
SOX3 SRY (sex determining region Y)-box 3
WNT3 wingless-type MMTV integration site family, member 3