absent cochlear outer hair cells Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the columnar outer hair sensory cells of the organ of Corti (Mammalian Phenotype Ontology, MP_0004403)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004403
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Genes

8 gene mutations causing the absent cochlear outer hair cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACAN aggrecan
CLRN1 clarin 1
COL11A1 collagen, type XI, alpha 1
CYS1 cystin 1
FGFR1 fibroblast growth factor receptor 1
LOC102723475 putative uncharacterized protein LOC388820
SLC12A7 solute carrier family 12 (potassium/chloride transporter), member 7
TMPRSS3 transmembrane protease, serine 3