nonsyndromic hearing impairment Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description a form of hearing impairment that is not associated with visible abnormalities of the external ear or other signs and symptoms; the vast majority of hereditary hearing loss is nonsyndromic and can be associated with abnormalities of the middle ear and/or inner ear (Mammalian Phenotype Ontology, MP_0006328)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0006328
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Genes

4 gene mutations causing the nonsyndromic hearing impairment 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