cortical dysplasia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The presence of developmental dysplasia of the cerebral cortex. (Human Phenotype Ontology, HP_0002539)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002539
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Genes

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

Symbol Name
ARHGAP31 Rho GTPase activating protein 31
ASNS asparagine synthetase (glutamine-hydrolyzing)
ASPM asp (abnormal spindle) homolog, microcephaly associated (Drosophila)
B3GNT1
HSD17B4 hydroxysteroid (17-beta) dehydrogenase 4
SNAP29 synaptosomal-associated protein, 29kDa
TUBB tubulin, beta class I
TUBB2B tubulin, beta 2B class IIb