dysmetria Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A type of ataxia characterized by the inability to carry out movements with the correct range and motion across the plane of more than one joint related to incorrect estimation of the distances required for targeted movements. (Human Phenotype Ontology, HP_0001310)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003314
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Genes

2 gene mutations causing the dysmetria phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ATCAY ataxia, cerebellar, Cayman type
SPTBN4 spectrin, beta, non-erythrocytic 4