abnormal pallium development Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the progression of the formation of the roof region of the telencephalon (Mammalian Phenotype Ontology, MP_0004171)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004171
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4 gene mutations causing the abnormal pallium development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADGRA2 adhesion G protein-coupled receptor A2
EMX2 empty spiracles homeobox 2
NR2E1 nuclear receptor subfamily 2, group E, member 1
PAX6 paired box 6