abnormality of cochlea Gene Set
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
|
