abnormal trigeminal nerve morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the chief sensory nerve of the face and motor nerve of the muscles of mastication; has three major divisions: ophthalmic, maxillary and mandibular (Mammalian Phenotype Ontology, MP_0001065)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001065
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Genes

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

Symbol Name
ARHGAP35 Rho GTPase activating protein 35
BDNF brain-derived neurotrophic factor
CERS2 ceramide synthase 2
CYP26A1 cytochrome P450, family 26, subfamily A, polypeptide 1
DLX2 distal-less homeobox 2
EDNRA endothelin receptor type A
EGR2 early growth response 2
ERBB2 erb-b2 receptor tyrosine kinase 2
ERBB3 erb-b2 receptor tyrosine kinase 3
ERBB4 erb-b2 receptor tyrosine kinase 4
GBX2 gastrulation brain homeobox 2
GDF15 growth differentiation factor 15
GFRA1 GDNF family receptor alpha 1
GRIN1 glutamate receptor, ionotropic, N-methyl D-aspartate 1
LMO4 LIM domain only 4
MEGF8 multiple EGF-like-domains 8
NEO1 neogenin 1
NEUROG1 neurogenin 1
NPR2 natriuretic peptide receptor 2
NRG1 neuregulin 1
NRP1 neuropilin 1
NRP2 neuropilin 2
OTX2 orthodenticle homeobox 2
PHOX2B paired-like homeobox 2b
PLXNA3 plexin A3
PLXNA4 plexin A4
POU4F1 POU class 4 homeobox 1
RELA v-rel avian reticuloendotheliosis viral oncogene homolog A
SEMA3A sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A
TBX1 T-box 1
TCOF1 Treacher Collins-Franceschetti syndrome 1
TUBB3 tubulin, beta 3 class III