Labyrinthitis Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores 2025
Category disease or phenotype associations
Type disease
Description A inner ear infectious disease which involves inflammation of the labyrinths. (Human Disease Ontology, DOID_1468)
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Genes

38 genes co-occuring with the disease Labyrinthitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Symbol Name Standardized Value
COCH cochlin 2.158
GJB2 gap junction protein, beta 2, 26kDa 1.956
MYO7A myosin VIIA 1.759
SRP72 signal recognition particle 72kDa 1.588
SLC26A4 solute carrier family 26 (anion exchanger), member 4 1.586
OC90 otoconin 90 1.586
GJB6 gap junction protein, beta 6, 30kDa 1.542
ATOH1 atonal homolog 1 (Drosophila) 1.479
NF2 neurofibromin 2 (merlin) 1.474
TNF tumor necrosis factor 1.419
IL1B interleukin 1, beta 1.413
GYPC glycophorin C (Gerbich blood group) 1.393
CRP C-reactive protein, pentraxin-related 1.357
IL6 interleukin 6 1.29
ACE2 angiotensin I converting enzyme 2 1.267
OTOF otoferlin 1.198
ADA2 adenosine deaminase 2 1.158
NTF3 neurotrophin 3 1.144
IL1A interleukin 1, alpha 1.136
TECTA tectorin alpha 1.11
SCGN secretagogin, EF-hand calcium binding protein 1.108
CLCNKA chloride channel, voltage-sensitive Ka 1.1
NOX3 NADPH oxidase 3 1.096
SHANK1 SH3 and multiple ankyrin repeat domains 1 1.095
DOLK dolichol kinase 1.092
TLR2 toll-like receptor 2 1.085
CTBP2 C-terminal binding protein 2 1.084
PRTN3 proteinase 3 1.08
IFNG interferon, gamma 1.052
ACE angiotensin I converting enzyme 1.047
BDNF brain-derived neurotrophic factor 1.045
IL10 interleukin 10 1.038
KCNJ10 potassium channel, inwardly rectifying subfamily J, member 10 1.033
CNTNAP4 contactin associated protein-like 4 1.023
NR3C2 nuclear receptor subfamily 3, group C, member 2 1.014
OTOG otogelin 1.011
ICAM1 intercellular adhesion molecule 1 1.006
TMC1 transmembrane channel-like 1 1.001