Malformations of Cortical Development Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D054220
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Genes

12 genes/proteins associated with the disease Malformations of Cortical Development from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
MTOR mechanistic target of rapamycin (serine/threonine kinase) 2.88009
SLC1A1 solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1 2.88009
KIF5C kinesin family member 5C 2.88009
TUBB2B tubulin, beta 2B class IIb 2.88009
PIK3CA phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit alpha 2.88009
NDST1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 2.88009
AKT3 v-akt murine thymoma viral oncogene homolog 3 2.88009
DYNC1H1 dynein, cytoplasmic 1, heavy chain 1 2.88009
KIF2A kinesin heavy chain member 2A 2.88009
TUBG1 tubulin, gamma 1 2.88009
KIF1BP KIF1 binding protein 2.88009
DHRS3 dehydrogenase/reductase (SDR family) member 3 1.01587