increased sensory neuron number Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description greater than normal numbers of cells that innervate an effector (muscle or glandular) tissue and are responsible for transmission of sensory impulses (Mammalian Phenotype Ontology, MP_0006006)
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36 gene mutations causing the increased sensory neuron number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ATOH7 atonal homolog 7 (Drosophila)
BARHL2 BarH-like homeobox 2
BAX BCL2-associated X protein
CDKN1B cyclin-dependent kinase inhibitor 1B (p27, Kip1)
CHD7 chromodomain helicase DNA binding protein 7
DFNA5 deafness, autosomal dominant 5
DSCAM Down syndrome cell adhesion molecule
DSCAML1 Down syndrome cell adhesion molecule like 1
EMX2 empty spiracles homeobox 2
EYA1 EYA transcriptional coactivator and phosphatase 1
FGFR1 fibroblast growth factor receptor 1
FGFR3 fibroblast growth factor receptor 3
FOXN4 forkhead box N4
GDF11 growth differentiation factor 11
GFI1 growth factor independent 1 transcription repressor
HES1 hes family bHLH transcription factor 1
HES5 hes family bHLH transcription factor 5
JAG1 jagged 1
JAG2 jagged 2
KIF5C kinesin family member 5C
NEUROD1 neuronal differentiation 1
NGFR nerve growth factor receptor
NOG noggin
NOTCH1 notch 1
NR2F1 nuclear receptor subfamily 2, group F, member 1
NRL neural retina leucine zipper
PANX1 pannexin 1
PDCD1 programmed cell death 1
POU4F2 POU class 4 homeobox 2
PRPH2 peripherin 2 (retinal degeneration, slow)
PTF1A pancreas specific transcription factor, 1a
PTK7 protein tyrosine kinase 7 (inactive)
RORB RAR-related orphan receptor B
SIX1 SIX homeobox 1
SPRY2 sprouty homolog 2 (Drosophila)
VANGL2 VANGL planar cell polarity protein 2