abnormal amygdala morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the almond-shaped body of basal nuclei anterior to the inferior horn of the lateral ventricle of the brain, within the temporal lobe; this area is involved in aggression and fear responses (Mammalian Phenotype Ontology, MP_0000818)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000818
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Genes

9 gene mutations causing the abnormal amygdala morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AGTR1 angiotensin II receptor, type 1
AGTR2 angiotensin II receptor, type 2
ATP1A2 ATPase, Na+/K+ transporting, alpha 2 polypeptide
GM2A GM2 ganglioside activator
MANBA mannosidase, beta A, lysosomal
NAGLU N-acetylglucosaminidase, alpha
NR2E1 nuclear receptor subfamily 2, group E, member 1
NTRK2 neurotrophic tyrosine kinase, receptor, type 2
ZIC2 Zic family member 2