thickened cerebral cortex Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description increased depth of the mantle covering the surface of the cerebral hemispheres (Mammalian Phenotype Ontology, MP_0000789)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000789
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Genes

6 gene mutations causing the thickened cerebral cortex phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
APAF1 apoptotic peptidase activating factor 1
CD81 CD81 molecule
CUX2 cut-like homeobox 2
FARP2 FERM, RhoGEF and pleckstrin domain protein 2
FGF2 fibroblast growth factor 2 (basic)
SMARCA1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 1