abnormal skeletal muscle mechanoreceptor morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the receptors that respond to mechanical pressure or distortion in the skeletal muscle (Mammalian Phenotype Ontology, MP_0000990)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000990
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14 gene mutations causing the abnormal skeletal muscle mechanoreceptor 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