midbrain hyperplasia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description overdevelopment or increased size, usually due an increased number of cells associated with the brain region derived from the middle of the three cerebral vesicles of the embryo; this region controls sensory and motor functions in the adult, including eye movement and coordination of auditory and visual reflexes (Mammalian Phenotype Ontology, MP_0000898)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000898
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Genes

3 gene mutations causing the midbrain hyperplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
APAF1 apoptotic peptidase activating factor 1
CYCS cytochrome c, somatic
IFT88 intraflagellar transport 88