abnormal muscle spindle morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the sensory organs in muscle that are involved in the stretch reflex (Mammalian Phenotype Ontology, MP_0004069)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004069
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Genes

14 gene mutations causing the abnormal muscle spindle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BACE1 beta-site APP-cleaving enzyme 1
DST dystonin
EGR3 early growth response 3
ERBB2 erb-b2 receptor tyrosine kinase 2
ETV1 ets variant 1
GDNF glial cell derived neurotrophic factor
GFRA1 GDNF family receptor alpha 1
NGFR nerve growth factor receptor
NRG1 neuregulin 1
NTF3 neurotrophin 3
NTRK1 neurotrophic tyrosine kinase, receptor, type 1
RET ret proto-oncogene
RUNX3 runt-related transcription factor 3
SHC1 SHC (Src homology 2 domain containing) transforming protein 1
Funding