progressive hearing impairment Gene Set
Genes
19 genes associated with the progressive hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol |
Name |
|
ACTG1
|
actin gamma 1
|
|
ALMS1
|
Alstrom syndrome protein 1
|
|
C10ORF2
|
chromosome 10 open reading frame 2
|
|
DFNA5
|
deafness, autosomal dominant 5
|
|
DIAPH1
|
diaphanous-related formin 1
|
|
LARS2
|
leucyl-tRNA synthetase 2, mitochondrial
|
|
MIR96
|
microRNA 96
|
|
MPZ
|
myelin protein zero
|
|
MYH14
|
myosin, heavy chain 14, non-muscle
|
|
MYH9
|
myosin, heavy chain 9, non-muscle
|
|
MYO3A
|
myosin IIIA
|
|
NLRP3
|
NLR family, pyrin domain containing 3
|
|
OPA1
|
optic atrophy 1 (autosomal dominant)
|
|
PEX11B
|
peroxisomal biogenesis factor 11 beta
|
|
POU3F4
|
POU class 3 homeobox 4
|
|
SERPINB6
|
serpin peptidase inhibitor, clade B (ovalbumin), member 6
|
|
SYNE4
|
spectrin repeat containing, nuclear envelope family member 4
|
|
TIMM8A
|
translocase of inner mitochondrial membrane 8 homolog A (yeast)
|
|
WFS1
|
Wolfram syndrome 1 (wolframin)
|
