abnormality of the middle ear ossicles Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the middle-ear ossicles (three small bones called malleus, incus, and stapes) that are contained within the middle ear and serve to transmit sounds from the air to the fluid-filled labyrinth (cochlea). (Human Phenotype Ontology, HP_0004452)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0004452
Similar Terms
Downloads & Tools

Genes

5 genes associated with the abnormality of the middle ear ossicles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
COL1A1 collagen, type I, alpha 1
COL1A2 collagen, type I, alpha 2
NOG noggin
POU3F4 POU class 3 homeobox 4
TFAP2A transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)