increased cochlear outer hair cell number Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description increased number (or more than the expected 3 rows) of the columnar outer hair sensory cells of the organ of Corti (Mammalian Phenotype Ontology, MP_0004401)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004401
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Genes

15 gene mutations causing the increased cochlear outer 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
FGFR3 fibroblast growth factor receptor 3
HES1 hes family bHLH transcription factor 1
HES5 hes family bHLH transcription factor 5
JAG2 jagged 2
NOG noggin
NOTCH1 notch 1
NR2F1 nuclear receptor subfamily 2, group F, member 1
PTK7 protein tyrosine kinase 7 (inactive)
SPRY2 sprouty homolog 2 (Drosophila)
VANGL2 VANGL planar cell polarity protein 2