abnormality of the cerebral cortex Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the cerebral cortex. (Human Phenotype Ontology, HP_0002538)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0002538
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7 genes associated with the abnormality of the cerebral cortex phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
WNT16 wingless-type MMTV integration site family, member 16 1.75294
FAM3C family with sequence similarity 3, member C 1.74041
CPED1 cadherin-like and PC-esterase domain containing 1 1.36886
GNL3 guanine nucleotide binding protein-like 3 (nucleolar) 1.28282
GPCPD1 glycerophosphocholine phosphodiesterase GDE1 homolog (S. cerevisiae) 1.27347
LOC100128714 uncharacterized LOC100128714 1.24751
FTO fat mass and obesity associated 0.942765