absent metencephalon Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the anterior part of the developing vertebrate hindbrain or the corresponding part of the adult brain normally composed of the cerebellum and the pons Varolii (Mammalian Phenotype Ontology, MP_0012516)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0012516
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Genes

2 gene mutations causing the absent metencephalon phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
OTX2 orthodenticle homeobox 2
WNT1 wingless-type MMTV integration site family, member 1