Dysphonia Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An impairment in the ability to produce voice sounds. (Human Phenotype Ontology, HP_0001618)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D055154
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Genes

19 genes/proteins associated with the disease Dysphonia from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
SLC22A2 solute carrier family 22 (organic cation transporter), member 2 1.52161
CYP3A4 cytochrome P450, family 3, subfamily A, polypeptide 4 1.26763
CCL2 chemokine (C-C motif) ligand 2 1.26113
CXCL8 chemokine (C-X-C motif) ligand 8 1.25682
ABCB1 ATP-binding cassette, sub-family B (MDR/TAP), member 1 1.24087
VEGFA vascular endothelial growth factor A 1.18226
EPX eosinophil peroxidase 1.16866
NR3C2 nuclear receptor subfamily 3, group C, member 2 1.16567
BCL2 B-cell CLL/lymphoma 2 1.16203
ABCG2 ATP-binding cassette, sub-family G (WHITE), member 2 (Junior blood group) 1.14336
CCNE1 cyclin E1 1.13109
CCNA2 cyclin A2 1.12391
PLA2G4A phospholipase A2, group IVA (cytosolic, calcium-dependent) 1.10033
TNF tumor necrosis factor 1.09892
HTR2A 5-hydroxytryptamine (serotonin) receptor 2A, G protein-coupled 1.09471
PLA1A phospholipase A1 member A 1.08407
CYP3A5 cytochrome P450, family 3, subfamily A, polypeptide 5 1.08161
HMGCS1 3-hydroxy-3-methylglutaryl-CoA synthase 1 (soluble) 1.05349
CCL4 chemokine (C-C motif) ligand 4 1.01852