absent cochlear inner hair cells Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the single row of flask-shaped inner hair sensory cells of the organ of Corti (Mammalian Phenotype Ontology, MP_0004397)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004397
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5 gene mutations causing the absent cochlear inner hair cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CLRN1 clarin 1
COL11A1 collagen, type XI, alpha 1
LOC102723475 putative uncharacterized protein LOC388820
SRRM4 serine/arginine repetitive matrix 4
TMPRSS3 transmembrane protease, serine 3