abnormality of the septum pellucidum Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the septum pellucidum, which is a thin, triangular, vertical membrane separating the lateral ventricles of the brain. (Human Phenotype Ontology, HP_0007375)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0007375
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22 genes associated with the abnormality of the septum pellucidum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
DOK7 docking protein 7
EZH2 enhancer of zeste 2 polycomb repressive complex 2 subunit
FGFR1 fibroblast growth factor receptor 1
FGFR2 fibroblast growth factor receptor 2
HCCS holocytochrome c synthase
HESX1 HESX homeobox 1
HYLS1 hydrolethalus syndrome 1
L1CAM L1 cell adhesion molecule
LHX3 LIM homeobox 3
LHX4 LIM homeobox 4
NSD1 nuclear receptor binding SET domain protein 1
OTX2 orthodenticle homeobox 2
PIGA phosphatidylinositol glycan anchor biosynthesis, class A
PIK3CA phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit alpha
POU1F1 POU class 1 homeobox 1
PROKR2 prokineticin receptor 2
PROP1 PROP paired-like homeobox 1
RAPSN receptor-associated protein of the synapse
RBM8A RNA binding motif protein 8A
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