abnormal facial nerve morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the sensory and motor nerve that supplies the muscles of facial expression and the expression and taste at the anterior two-thirds of the tongue; principal branches are the superficial opthalmic, buccal, palatine and hyomandibular (Mammalian Phenotype Ontology, MP_0001071)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001071
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Genes

26 gene mutations causing the abnormal facial nerve morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARHGAP35 Rho GTPase activating protein 35
CDK5 cyclin-dependent kinase 5
DLX1 distal-less homeobox 1
DLX2 distal-less homeobox 2
EDNRA endothelin receptor type A
EGR2 early growth response 2
ERBB4 erb-b2 receptor tyrosine kinase 4
EYA1 EYA transcriptional coactivator and phosphatase 1
GDF15 growth differentiation factor 15
GRB2 growth factor receptor-bound protein 2
HOXA1 homeobox A1
HOXA2 homeobox A2
HOXB1 homeobox B1
HOXB2 homeobox B2
MYH10 myosin, heavy chain 10, non-muscle
NEUROG2 neurogenin 2
NRP1 neuropilin 1
OTULIN OTU deubiquitinase with linear linkage specificity
PHOX2A paired-like homeobox 2a
PHOX2B paired-like homeobox 2b
PLXNA4 plexin A4
SIX1 SIX homeobox 1
SLC5A3 solute carrier family 5 (sodium/myo-inositol cotransporter), member 3
TBCE tubulin folding cofactor E
TBX1 T-box 1
TFAP2A transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)