sensorineural Gene Set

Dataset GeneRIF Biological Term Annotations
Category structural or functional annotations
Type biological term
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Genes

89 genes co-occuring with the biological term sensorineural in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Symbol Name
ACTG1 actin gamma 1
AK2 adenylate kinase 2
ANOS1 anosmin 1
ATP6V1B1 ATPase, H+ transporting, lysosomal 56/58kDa, V1 subunit B1
BSND barttin CLCNK-type chloride channel accessory beta subunit
C2ORF71 chromosome 2 open reading frame 71
CABP2 calcium binding protein 2
CDKN1C cyclin-dependent kinase inhibitor 1C (p57, Kip2)
CEP250 centrosomal protein 250kDa
CFH complement factor H
CLCNKA chloride channel, voltage-sensitive Ka
CLCNKB chloride channel, voltage-sensitive Kb
COCH cochlin
COL2A1 collagen, type II, alpha 1
COL9A3 collagen, type IX, alpha 3
COQ6 coenzyme Q6 monooxygenase
DFNA24 deafness, autosomal dominant 24
DFNA52 deafness, autosomal dominant 52
DFNB40 deafness, autosomal recessive 40
EDN1 endothelin 1
EYA4 EYA transcriptional coactivator and phosphatase 4
F2 coagulation factor II (thrombin)
F5 coagulation factor V (proaccelerin, labile factor)
FGF3 fibroblast growth factor 3
FGFR3 fibroblast growth factor receptor 3
GATA3 GATA binding protein 3
GIPC3 GIPC PDZ domain containing family, member 3
GJB2 gap junction protein, beta 2, 26kDa
GJB3 gap junction protein, beta 3, 31kDa
GJB6 gap junction protein, beta 6, 30kDa
GPSM2 G-protein signaling modulator 2
GSTM1 glutathione S-transferase mu 1
HARS2 histidyl-tRNA synthetase 2, mitochondrial
HGF hepatocyte growth factor (hepapoietin A; scatter factor)
HLA-DQB1 major histocompatibility complex, class II, DQ beta 1
HLA-DRB1 major histocompatibility complex, class II, DR beta 1
HMX2 H6 family homeobox 2
HMX3 H6 family homeobox 3
HSPA1A heat shock 70kDa protein 1A
HSPA1B heat shock 70kDa protein 1B
HSPA1L heat shock 70kDa protein 1-like
IL6 interleukin 6
ITGA2 integrin, alpha 2 (CD49B, alpha 2 subunit of VLA-2 receptor)
ITGB3 integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61)
KCNJ10 potassium channel, inwardly rectifying subfamily J, member 10
KCNQ1 potassium channel, voltage gated KQT-like subfamily Q, member 1
KCNQ4 potassium channel, voltage gated KQT-like subfamily Q, member 4
LHX3 LIM homeobox 3
LRTOMT leucine rich transmembrane and O-methyltransferase domain containing
MBL2 mannose-binding lectin (protein C) 2, soluble
MIF macrophage migration inhibitory factor (glycosylation-inhibiting factor)
MT-TS1 tRNA
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
MYH9 myosin, heavy chain 9, non-muscle
MYO15A myosin XVA
MYO1A myosin IA
MYO1C myosin IC
MYO1F myosin IF
MYO6 myosin VI
NGF nerve growth factor (beta polypeptide)
NLRP3 NLR family, pyrin domain containing 3
NOS3 nitric oxide synthase 3 (endothelial cell)
OPA1 optic atrophy 1 (autosomal dominant)
OTOG otogelin
OTOGL otogelin-like
P2RX2 purinergic receptor P2X, ligand gated ion channel, 2
PMP22 peripheral myelin protein 22
POLG polymerase (DNA directed), gamma
PRPS1 phosphoribosyl pyrophosphate synthetase 1
PTPRJ protein tyrosine phosphatase, receptor type, J
RFT1 RFT1 homolog (S. cerevisiae)
RNR2 RNA, ribosomal cluster 2
SERAC1 serine active site containing 1
SERPINB6 serpin peptidase inhibitor, clade B (ovalbumin), member 6
SLC19A2 solute carrier family 19 (thiamine transporter), member 2
SLC26A4 solute carrier family 26 (anion exchanger), member 4
SLC26A5 solute carrier family 26 (anion exchanger), member 5
SLC29A3 solute carrier family 29 (equilibrative nucleoside transporter), member 3
SMPX small muscle protein, X-linked
TBX2 T-box 2
TBX4 T-box 4
TECTA tectorin alpha
TMC1 transmembrane channel-like 1
TMIE transmembrane inner ear
TMPRSS3 transmembrane protease, serine 3
TXN thioredoxin
USH1C Usher syndrome 1C (autosomal recessive, severe)
USH2A Usher syndrome 2A (autosomal recessive, mild)
WFS1 Wolfram syndrome 1 (wolframin)