partial loss of secondary muscle spindle Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000996
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Genes

1 gene mutations causing the partial loss of secondary muscle spindle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ERBB2 erb-b2 receptor tyrosine kinase 2