abnormal cochlear hair cell development Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description atypical initial production, differentiation, migration or maturation of the sensory epithelial cells of the cochlea (Mammalian Phenotype Ontology, MP_0004589)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004589
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Genes

9 gene mutations causing the abnormal cochlear hair cell development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
FGF20 fibroblast growth factor 20
FGFR1 fibroblast growth factor receptor 1
GFI1 growth factor independent 1 transcription repressor
IGF1R insulin-like growth factor 1 receptor
MYO6 myosin VI
NR2F1 nuclear receptor subfamily 2, group F, member 1
POU4F3 POU class 4 homeobox 3
SRRM4 serine/arginine repetitive matrix 4
TRIOBP TRIO and F-actin binding protein