absent primary muscle spindle Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description missing sensory organ in muscle; involved in the stretch reflex and is sensitive to stretch velocity (Mammalian Phenotype Ontology, MP_0000992)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000992
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1 gene mutations causing the absent primary muscle spindle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ERBB2 erb-b2 receptor tyrosine kinase 2