abnormal anterior commissure pars posterior morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the large posterior part of the anterior commissure which connects the right and left temporal lobes (Mammalian Phenotype Ontology, MP_0010860)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010860
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Genes

9 gene mutations causing the abnormal anterior commissure pars posterior morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARHGAP35 Rho GTPase activating protein 35
EBF1 early B-cell factor 1
EFNB2 ephrin-B2
EPHA4 EPH receptor A4
EPHB2 EPH receptor B2
MAP3K12 mitogen-activated protein kinase kinase kinase 12
MAPK8IP3 mitogen-activated protein kinase 8 interacting protein 3
NRP2 neuropilin 2
PLXNA4 plexin A4