abnormal innervation pattern to muscle Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any changes in the placement, morphology or number of sensory, sympathetic or motor nerves to targets in muscle (Mammalian Phenotype Ontology, MP_0001052)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001052
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27 gene mutations causing the abnormal innervation pattern to muscle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AGRN agrin
CACNA1S calcium channel, voltage-dependent, L type, alpha 1S subunit
CHAT choline O-acetyltransferase
CHRNA1 cholinergic receptor, nicotinic, alpha 1 (muscle)
CHRNG cholinergic receptor, nicotinic, gamma (muscle)
CLIP3 CAP-GLY domain containing linker protein 3
CLP1 cleavage and polyadenylation factor I subunit 1
DOK7 docking protein 7
ECEL1 endothelin converting enzyme-like 1
EEF1A2 eukaryotic translation elongation factor 1 alpha 2
EPHA4 EPH receptor A4
ERBB2 erb-b2 receptor tyrosine kinase 2
ETV1 ets variant 1
ETV4 ets variant 4
GARS glycyl-tRNA synthetase
GDNF glial cell derived neurotrophic factor
GFRA1 GDNF family receptor alpha 1
IGHMBP2 immunoglobulin mu binding protein 2
LMNB1 lamin B1
MUSK muscle, skeletal, receptor tyrosine kinase
NGFR nerve growth factor receptor
NTF3 neurotrophin 3
NTF4 neurotrophin 4
RET ret proto-oncogene
SCYL1 SCY1-like 1 (S. cerevisiae)
TOP2B topoisomerase (DNA) II beta 180kDa
UNC5C unc-5 homolog C (C. elegans)