increased midbrain size Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description greater than average size of 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_0012091)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0012091
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Genes

7 gene mutations causing the increased midbrain size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
APAF1 apoptotic peptidase activating factor 1
CASP9 caspase 9, apoptosis-related cysteine peptidase
CYCS cytochrome c, somatic
IFT88 intraflagellar transport 88
KDM2B lysine (K)-specific demethylase 2B
PAK1IP1 PAK1 interacting protein 1
SIX3 SIX homeobox 3