abnormal cholinergic neuron morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the neurons that utilize acetylcholine as a neurotransmitter, including include alpha-motor neurons of the spinal cord, cranial nerves innervating skeletal muscle, preganglionic sympathetic and postganglionic parasympathetic neurons (Mammalian Phenotype Ontology, MP_0001038)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001038
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Genes

8 gene mutations causing the abnormal cholinergic neuron morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARX aristaless related homeobox
EGR3 early growth response 3
GDNF glial cell derived neurotrophic factor
LHX8 LIM homeobox 8
NGFR nerve growth factor receptor
NTRK1 neurotrophic tyrosine kinase, receptor, type 1
OTC ornithine carbamoyltransferase
SORL1 sortilin-related receptor, L(DLR class) A repeats containing