cochlear malformation Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The presence of a malformed cochlea. (Human Phenotype Ontology, HP_0008554)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008554
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Genes

6 genes associated with the cochlear malformation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
COL4A6 collagen, type IV, alpha 6
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