absent red nucleus Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the pale pink structure located in the tegmentum of the midbrain next to the substantia nigra and involved in motor coordination (Mammalian Phenotype Ontology, MP_0012268)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0012268
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Genes

1 gene mutations causing the absent red nucleus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
POU4F1 POU class 4 homeobox 1