decreased cochlear inner hair cell number Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description decreased number (or less than the expected single row) of the flask-shaped inner hair sensory cells of the organ of Corti (Mammalian Phenotype Ontology, MP_0004396)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004396
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Genes

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

Symbol Name
CDH23 cadherin-related 23
CDKN2D cyclin-dependent kinase inhibitor 2D (p19, inhibits CDK4)
CLRN1 clarin 1
COL11A1 collagen, type XI, alpha 1
HR hair growth associated
IGF1R insulin-like growth factor 1 receptor
LOC102723475 putative uncharacterized protein LOC388820
SIX1 SIX homeobox 1
SLC12A2 solute carrier family 12 (sodium/potassium/chloride transporter), member 2
SLC17A8 solute carrier family 17 (vesicular glutamate transporter), member 8
SRRM4 serine/arginine repetitive matrix 4
TMPRSS3 transmembrane protease, serine 3