abnormal facial motor nucleus morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the group of motor neurons residing in the pons that innervate the muscles of facial expression (Mammalian Phenotype Ontology, MP_0000909)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000909
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Genes

14 gene mutations causing the abnormal facial motor nucleus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BAX BCL2-associated X protein
BCL2 B-cell CLL/lymphoma 2
CASP2 caspase 2, apoptosis-related cysteine peptidase
CLCF1 cardiotrophin-like cytokine factor 1
CNTFR ciliary neurotrophic factor receptor
HOXA1 homeobox A1
HOXA2 homeobox A2
HOXB1 homeobox B1
HOXB2 homeobox B2
NMNAT2 nicotinamide nucleotide adenylyltransferase 2
NRP1 neuropilin 1
NTRK2 neurotrophic tyrosine kinase, receptor, type 2
PHOX2B paired-like homeobox 2b
VEGFA vascular endothelial growth factor A