absent septum pellucidum Gene Set
Genes
19 genes associated with the absent 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
|
|
OTX2
|
orthodenticle homeobox 2
|
|
PIGA
|
phosphatidylinositol glycan anchor biosynthesis, class A
|
|
POU1F1
|
POU class 1 homeobox 1
|
|
PROKR2
|
prokineticin receptor 2
|
|
PROP1
|
PROP paired-like homeobox 1
|
|
RAPSN
|
receptor-associated protein of the synapse
|
|
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
|
