increased cochlear hair cell number Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description increased number of the sensory epithelial cells of the cochlea, which are normally in synaptic contact with the auditory nerve (Mammalian Phenotype Ontology, MP_0004407)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004407
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Genes

18 gene mutations causing the increased cochlear hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CDKN1B cyclin-dependent kinase inhibitor 1B (p27, Kip1)
CHD7 chromodomain helicase DNA binding protein 7
DFNA5 deafness, autosomal dominant 5
EMX2 empty spiracles homeobox 2
EYA1 EYA transcriptional coactivator and phosphatase 1
FGFR1 fibroblast growth factor receptor 1
FGFR3 fibroblast growth factor receptor 3
HES1 hes family bHLH transcription factor 1
HES5 hes family bHLH transcription factor 5
JAG1 jagged 1
JAG2 jagged 2
NOG noggin
NOTCH1 notch 1
NR2F1 nuclear receptor subfamily 2, group F, member 1
PTK7 protein tyrosine kinase 7 (inactive)
SIX1 SIX homeobox 1
SPRY2 sprouty homolog 2 (Drosophila)
VANGL2 VANGL planar cell polarity protein 2