partial agenesis of the corpus callosum Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A partial failure of the development of the corpus callosum. (Human Phenotype Ontology, HP_0001338)
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12 genes associated with the partial agenesis of the corpus callosum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AMER1 APC membrane recruitment protein 1
DHCR24 24-dehydrocholesterol reductase
GLI2 GLI family zinc finger 2
GPSM2 G-protein signaling modulator 2
ISPD isoprenoid synthase domain containing
L1CAM L1 cell adhesion molecule
LRP2 low density lipoprotein receptor-related protein 2
MED12 mediator complex subunit 12
MPLKIP M-phase specific PLK1 interacting protein
NSD1 nuclear receptor binding SET domain protein 1
PDHX pyruvate dehydrogenase complex, component X
SLC25A19 solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19