Hearing Loss, Sudden Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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Genes

31 genes associated with the Hearing Loss, Sudden phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
CCL2 chemokine (C-C motif) ligand 2
CFH complement factor H
CYP1A1 cytochrome P450, family 1, subfamily A, polypeptide 1
F2 coagulation factor II (thrombin)
F5 coagulation factor V (proaccelerin, labile factor)
GJB2 gap junction protein, beta 2, 26kDa
GPX1 glutathione peroxidase 1
GSTM1 glutathione S-transferase mu 1
GSTT1 glutathione S-transferase theta 1
HLA-DQB1 major histocompatibility complex, class II, DQ beta 1
HLA-DRB1 major histocompatibility complex, class II, DR beta 1
HSPA1A heat shock 70kDa protein 1A
IL1A interleukin 1, alpha
IL1B interleukin 1, beta
IL4R interleukin 4 receptor
IL6 interleukin 6
ITGA1 integrin, alpha 1
ITGA2 integrin, alpha 2 (CD49B, alpha 2 subunit of VLA-2 receptor)
ITGA3 integrin, alpha 3 (antigen CD49C, alpha 3 subunit of VLA-3 receptor)
ITGB3 integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61)
MMP1 matrix metallopeptidase 1
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
MTR 5-methyltetrahydrofolate-homocysteine methyltransferase
PLAT plasminogen activator, tissue
PON1 paraoxonase 1
PON2 paraoxonase 2
PRKCH protein kinase C, eta
PROCR protein C receptor, endothelial
SELE selectin E
SERPINE1 serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1
SOD2 superoxide dismutase 2, mitochondrial