Sensory Hearing Loss Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C1691779
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Genes

14 genes associated with the disease Sensory Hearing Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ACTB actin, beta
COL11A2 collagen, type XI, alpha 2
COL2A1 collagen, type II, alpha 1
COL9A1 collagen, type IX, alpha 1
FADD Fas (TNFRSF6)-associated via death domain
FGF3 fibroblast growth factor 3
GJB2 gap junction protein, beta 2, 26kDa
GJB3 gap junction protein, beta 3, 31kDa
IRX5 iroquois homeobox 5
LRP2 low density lipoprotein receptor-related protein 2
NPL N-acetylneuraminate pyruvate lyase (dihydrodipicolinate synthase)
OPA1 optic atrophy 1 (autosomal dominant)
SLC26A4 solute carrier family 26 (anion exchanger), member 4
SOBP sine oculis binding protein homolog (Drosophila)