Abnormal Cochlea Morphology Gene Set
Genes
15 genes associated with the disease Abnormal Cochlea Morphology in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
| Symbol |
Name |
|
ARSG
|
arylsulfatase G
|
|
CDH23
|
cadherin-related 23
|
|
CEP78
|
centrosomal protein 78kDa
|
|
CIB2
|
calcium and integrin binding family member 2
|
|
CLRN1
|
clarin 1
|
|
COG4
|
component of oligomeric golgi complex 4
|
|
HARS1
|
histidyl-tRNA synthetase 1
|
|
MYO7A
|
myosin VIIA
|
|
NDP
|
Norrie disease (pseudoglioma)
|
|
PCDH15
|
protocadherin-related 15
|
|
POU3F4
|
POU class 3 homeobox 4
|
|
SETBP1
|
SET binding protein 1
|
|
TIMM8A
|
translocase of inner mitochondrial membrane 8 homolog A (yeast)
|
|
USH1C
|
Usher syndrome 1C (autosomal recessive, severe)
|
|
USH1G
|
Usher syndrome 1G (autosomal recessive)
|
