morphological abnormality of the middle ear Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the morphology or structure of the middle ear. (Human Phenotype Ontology, HP_0008609)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008609
Similar Terms
Downloads & Tools

Genes

10 genes associated with the morphological abnormality of the middle ear 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
EYA1 EYA transcriptional coactivator and phosphatase 1
FRAS1 Fraser extracellular matrix complex subunit 1
FREM2 FRAS1 related extracellular matrix protein 2
GRIP1 glutamate receptor interacting protein 1
NOG noggin
POU3F4 POU class 3 homeobox 4
RAI1 retinoic acid induced 1
TFAP2A transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)
Funding