conductive hearing impairment Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of vibrational conductance of sound to the inner ear leading to impairment of sensory perception of sound. (Human Phenotype Ontology, HP_0000405)
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13 gene mutations causing the conductive hearing impairment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
DLX1 distal-less homeobox 1
DNAJC5 DnaJ (Hsp40) homolog, subfamily C, member 5
EMX2 empty spiracles homeobox 2
EYA1 EYA transcriptional coactivator and phosphatase 1
NAGLU N-acetylglucosaminidase, alpha
NOG noggin
POU3F4 POU class 3 homeobox 4
RPL38 ribosomal protein L38
SALL1 spalt-like transcription factor 1
SALL4 spalt-like transcription factor 4
SIX1 SIX homeobox 1
TFAP2A transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)
TGIF1 TGFB-induced factor homeobox 1