abnormal phrenic nerve morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of motor, sensory and sympathetic neuron axons that project to the diaphragm and other tissues (Mammalian Phenotype Ontology, MP_0001078)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001078
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19 gene mutations causing the abnormal phrenic nerve morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BAX BCL2-associated X protein
CACNA1S calcium channel, voltage-dependent, L type, alpha 1S subunit
CHAT choline O-acetyltransferase
CHRNG cholinergic receptor, nicotinic, gamma (muscle)
CLIP3 CAP-GLY domain containing linker protein 3
CLP1 cleavage and polyadenylation factor I subunit 1
ECEL1 endothelin converting enzyme-like 1
EDNRB endothelin receptor type B
ERBB2 erb-b2 receptor tyrosine kinase 2
LMNB1 lamin B1
LRP4 low density lipoprotein receptor-related protein 4
MYCBP2 MYC binding protein 2, E3 ubiquitin protein ligase
NRG1 neuregulin 1
POU3F1 POU class 3 homeobox 1
SCARB2 scavenger receptor class B, member 2
SLC5A3 solute carrier family 5 (sodium/myo-inositol cotransporter), member 3
TBCE tubulin folding cofactor E
UNC5C unc-5 homolog C (C. elegans)
VEGFA vascular endothelial growth factor A