|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||missing a portion of the sensory organ in muscle; involved in the stretch reflex and is not sensitive to stretch velocity (Mammalian Phenotype Ontology, MP_0000996)|
|Downloads & Tools|
1 gene mutations causing the partial loss of secondary muscle spindle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
|ERBB2||erb-b2 receptor tyrosine kinase 2|