abnormal cochlear viii nucleus morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of two paired brainstem nuclei, the dorsal cochlear nucleus and the ventral cochlear nucleus, that lie dorsal and ventral, respectively, to the inferior cerebellar peduncle at the rostral pole of the medulla; the cochlear nuclei receive input from the cochlear nerve and send projections to the inferior colliculus, the medial geniculate, and other forebrain structures (Mammalian Phenotype Ontology, MP_0012490)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0012490
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Genes

9 gene mutations causing the abnormal cochlear viii nucleus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AGTPBP1 ATP/GTP binding protein 1
ATOH1 atonal homolog 1 (Drosophila)
ATP2B2 ATPase, Ca++ transporting, plasma membrane 2
GRID2 glutamate receptor, ionotropic, delta 2
HOXB1 homeobox B1
HOXB2 homeobox B2
IL17RD interleukin 17 receptor D
KCNJ6 potassium channel, inwardly rectifying subfamily J, member 6
RORA RAR-related orphan receptor A