abnormality of cochlea Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the cochlea. (Human Phenotype Ontology, HP_0000375)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000375
Similar Terms
Downloads & Tools

Genes

8 genes associated with the abnormality of cochlea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
COCH cochlin
COL4A6 collagen, type IV, alpha 6
DDX11 DEAD/H (Asp-Glu-Ala-Asp/His) box helicase 11
EYA1 EYA transcriptional coactivator and phosphatase 1
FOXI1 forkhead box I1
KCNJ10 potassium channel, inwardly rectifying subfamily J, member 10
ORC1 origin recognition complex, subunit 1
SLC26A4 solute carrier family 26 (anion exchanger), member 4