abnormal cerebellum dentate nucleus morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the largest and most lateral of the deep cerebellum nuclei; it receives axons of Purkinje cells in the lateral cerebellar hemisphere (neocerebellum) and receives its afferents from the premotor cortex and the supplementary motor cortex through the pontocerebellar system, and its efferents project through the superior cerebellar peduncle and is a major source of its fibers (Mammalian Phenotype Ontology, MP_0009980)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009980
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Genes

1 gene mutations causing the abnormal cerebellum dentate nucleus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
SLC9A1 solute carrier family 9, subfamily A (NHE1, cation proton antiporter 1), member 1