abnormal frontal lobe morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the anterior part of the cerebral hemisphere (Mammalian Phenotype Ontology, MP_0000798)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000798
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10 gene mutations causing the abnormal frontal lobe morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ATP7B ATPase, Cu++ transporting, beta polypeptide
CHD7 chromodomain helicase DNA binding protein 7
FES FES proto-oncogene, tyrosine kinase
FGF2 fibroblast growth factor 2 (basic)
MANBA mannosidase, beta A, lysosomal
MAPK8IP3 mitogen-activated protein kinase 8 interacting protein 3
MECP2 methyl CpG binding protein 2
RB1 retinoblastoma 1
SOD2 superoxide dismutase 2, mitochondrial
WNT1 wingless-type MMTV integration site family, member 1