small trigeminal ganglion Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduced size of the trigeminal ganglion (Mammalian Phenotype Ontology, MP_0001093)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001093
Similar Terms
Downloads & Tools

Genes

14 gene mutations causing the small trigeminal ganglion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BDNF brain-derived neurotrophic factor
DLX5 distal-less homeobox 5
EFNB2 ephrin-B2
MECOM MDS1 and EVI1 complex locus
MYCN v-myc avian myelocytomatosis viral oncogene neuroblastoma derived homolog
NTF3 neurotrophin 3
NTRK1 neurotrophic tyrosine kinase, receptor, type 1
NTRK2 neurotrophic tyrosine kinase, receptor, type 2
NTRK3 neurotrophic tyrosine kinase, receptor, type 3
PHOX2A paired-like homeobox 2a
PHOX2B paired-like homeobox 2b
POU4F1 POU class 4 homeobox 1
TCOF1 Treacher Collins-Franceschetti syndrome 1
TFAP2A transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)