nonsyndromic hearing loss Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An auditory system disease that is associated with permanent hearing loss caused by damage to structures in the inner ear and/or the middle ear, which is not associated with other signs and symptoms. (Human Disease Ontology, DOID_0050563)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004749
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Genes

4 gene mutations causing the nonsyndromic hearing loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CDKN2D cyclin-dependent kinase inhibitor 2D (p19, inhibits CDK4)
CEACAM16 carcinoembryonic antigen-related cell adhesion molecule 16
COL11A2 collagen, type XI, alpha 2
SLC26A4 solute carrier family 26 (anion exchanger), member 4