absent cerebral aqueduct Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the channel in the mesencephalon that connects the third and fourth ventricles (Mammalian Phenotype Ontology, MP_0013000)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0013000
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1 gene mutations causing the absent cerebral aqueduct phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
KDM2B lysine (K)-specific demethylase 2B