|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||missing sensory organ in muscle; involved in the stretch reflex and is sensitive to stretch velocity (Mammalian Phenotype Ontology, MP_0000992)|
|Downloads & Tools|
1 gene mutations causing the absent primary muscle spindle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
|ERBB2||erb-b2 receptor tyrosine kinase 2|