Mild Neurosensory Hearing Impairment Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description The presence of a mild form of sensorineural hearing impairment. (Human Phenotype Ontology, HP_0008587)
External Link https://www.disgenet.org/browser/0/1/0/C4021538
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Genes

35 genes associated with the disease Mild Neurosensory Hearing Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ACSL4 acyl-CoA synthetase long-chain family member 4
AGTR2 angiotensin II receptor, type 2
ALG13 ALG13, UDP-N-acetylglucosaminyltransferase subunit
ARHGEF6 Rac/Cdc42 guanine nucleotide exchange factor (GEF) 6
ARX aristaless related homeobox
CLCN4 chloride channel, voltage-sensitive 4
CNKSR2 connector enhancer of kinase suppressor of Ras 2
COL11A2 collagen, type XI, alpha 2
COL2A1 collagen, type II, alpha 1
DLG3 discs, large homolog 3 (Drosophila)
DMD dystrophin
FRMPD4 FERM and PDZ domain containing 4
FTSJ1 FtsJ RNA methyltransferase homolog 1 (E. coli)
GDI1 GDP dissociation inhibitor 1
HCFC1 host cell factor C1
IL1RAPL1 interleukin 1 receptor accessory protein-like 1
IQSEC2 IQ motif and Sec7 domain 2
MECP2 methyl CpG binding protein 2
MED12 mediator complex subunit 12
MID2 midline 2
PAK3 p21 protein (Cdc42/Rac)-activated kinase 3
PGM3 phosphoglucomutase 3
PTCHD1 patched domain containing 1
RAB39B RAB39B, member RAS oncogene family
RPS6KA3 ribosomal protein S6 kinase, 90kDa, polypeptide 3
SLC9A7 solute carrier family 9, subfamily A (NHE7, cation proton antiporter 7), member 7
STEEP1 STING1 ER exit protein 1
SYP synaptophysin
TSPAN7 tetraspanin 7
UPF3B UPF3 regulator of nonsense transcripts homolog B (yeast)
USP27X ubiquitin specific peptidase 27, X-linked
USP9X ubiquitin specific peptidase 9, X-linked
ZNF41 zinc finger protein 41
ZNF711 zinc finger protein 711
ZNF81 zinc finger protein 81