tinnitus Gene Set
Genes
16 genes associated with the tinnitus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol |
Name |
|
CACNA1A
|
calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
|
|
COCH
|
cochlin
|
|
DSPP
|
dentin sialophosphoprotein
|
|
JAK2
|
Janus kinase 2
|
|
KCNQ4
|
potassium channel, voltage gated KQT-like subfamily Q, member 4
|
|
MFN2
|
mitofusin 2
|
|
MPL
|
MPL proto-oncogene, thrombopoietin receptor
|
|
NAGA
|
N-acetylgalactosaminidase, alpha-
|
|
NF2
|
neurofibromin 2 (merlin)
|
|
P2RX2
|
purinergic receptor P2X, ligand gated ion channel, 2
|
|
SDHAF2
|
succinate dehydrogenase complex assembly factor 2
|
|
SDHB
|
succinate dehydrogenase complex, subunit B, iron sulfur (Ip)
|
|
SDHC
|
succinate dehydrogenase complex, subunit C, integral membrane protein, 15kDa
|
|
SDHD
|
succinate dehydrogenase complex, subunit D, integral membrane protein
|
|
TET2
|
tet methylcytosine dioxygenase 2
|
|
VHL
|
von Hippel-Lindau tumor suppressor, E3 ubiquitin protein ligase
|
