RGD DISEASE ONTOLOGY - ANNOTATIONS
RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.
Term: Hearing Loss, Noise-Induced
Accession: DOID:9002910
browse the term
Definition: Hearing loss due to exposure to explosive loud noise or chronic exposure to sound level greater than 85 dB. The hearing loss is often in the frequency range 4000-6000 hertz.
Synonyms: exact_synonym: Acoustic Trauma
related_synonym: Noise-induced hearing loss, association with; Noise-induced hearing loss, susceptibility to
primary_id: MESH:D006317
alt_id: MIM:613035
xref: EFO:1001254 ; EFO:1001338
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Arc
activity regulated cytoskeletal-associated protein
ISO
RGD
PMID:17275194
RGD:8655559
NCBI chr15:74,540,930...74,544,419
Ensembl chr15:74,540,932...74,544,419
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Bdnf
brain derived neurotrophic factor
IEP ISO IMP
protein:increased expression:cochlea:
RGD
PMID:19925854 PMID:17275194 PMID:22723694
RGD:8636263 , RGD:8655559 , RGD:8655575
NCBI chr 2:109,505,045...109,557,388
Ensembl chr 2:109,505,045...109,557,352
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Calb1
calbindin 1
ISO
RGD
PMID:22428005
RGD:401940127
NCBI chr 4:15,881,264...15,906,709
Ensembl chr 4:15,881,264...15,908,064
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Cat
catalase
susceptibility treatment severity
ISO IEP
DNA:SNPs,haplotype::
RGD
PMID:17567781 PMID:23179931 PMID:18212468
RGD:9068906 , RGD:9068923 , RGD:9190810
NCBI chr 2:103,284,249...103,315,498
Ensembl chr 2:103,284,194...103,315,505
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Ccl2
C-C motif chemokine ligand 2
IEP
mRNA:increased expression:cochlea (mouse)
RGD
PMID:17081714
RGD:8549464
NCBI chr11:81,926,403...81,928,278
Ensembl chr11:81,926,397...81,928,279
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Ccr2
C-C motif chemokine receptor 2
IMP
RGD
PMID:17075702
RGD:8657356
NCBI chr 9:123,901,954...123,913,594
Ensembl chr 9:123,901,987...123,913,594
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Cdh23
cadherin related 23 (otocadherin)
no_association
ISO
DNA:SNPs: :rs1227049, rs3802711 (human) DNA:SNPs: :rs1227049, rs1227051 (human)
RGD
PMID:16598924 PMID:16598924
RGD:8662283 , RGD:8662283
NCBI chr10:60,138,527...60,532,291
Ensembl chr10:60,138,527...60,532,269
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Cdkn1a
cyclin dependent kinase inhibitor 1A
IEP
RGD
PMID:21187137
RGD:8661793
NCBI chr17:29,309,953...29,319,696
Ensembl chr17:29,309,950...29,319,701
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Cfi
complement component factor i
ISO
mRNA:increased expression:spiral organ of cochlea, sensory epithelium
RGD
PMID:23727008
RGD:8662317
NCBI chr 3:129,630,432...129,668,978
Ensembl chr 3:129,629,533...129,668,981
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Cntn1
contactin 1
ISO
RGD
PMID:22044737
RGD:5685697
NCBI chr15:91,949,034...92,239,834
Ensembl chr15:91,949,046...92,239,848
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Gabra1
gamma-aminobutyric acid type A receptor subunit alpha 1
ISO
RGD
PMID:22428005
RGD:401940127
NCBI chr11:42,021,766...42,073,893
Ensembl chr11:42,021,766...42,073,757
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Gad1
glutamate decarboxylase 1
ISO
RGD
PMID:22428005
RGD:401940127
NCBI chr 2:70,392,109...70,432,358
Ensembl chr 2:70,383,416...70,432,358
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Gap43
growth associated protein 43
ISO
RGD
PMID:22428005
RGD:401940127
NCBI chr16:42,068,915...42,161,014
Ensembl chr16:42,068,805...42,161,014
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Gjb2
gap junction protein, beta 2
ISO
protein:increased expression:cochlea:
RGD
PMID:15224875
RGD:7349367
NCBI chr14:57,336,059...57,342,159
Ensembl chr14:57,336,057...57,342,159
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Gstm1
glutathione S-transferase, mu 1
susceptibility no_association
ISO
DNA:deletion, haplotype:cds (human) DNA:deletion:cds (human)
RGD
PMID:19643173 PMID:16535824
RGD:7488956 , RGD:7495798
NCBI chr 3:107,919,566...107,925,289
Ensembl chr 3:107,919,571...107,925,289
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Gstt1
glutathione S-transferase, theta 1
susceptibility no_association
ISO
DNA:deletion:cds (human)
RGD
PMID:16535824 PMID:15811702
RGD:7495798 , RGD:7794850
NCBI chr10:75,619,647...75,634,418
Ensembl chr10:75,619,647...75,634,418
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Hif1a
hypoxia inducible factor 1, alpha subunit
treatment
IDA
RGD
PMID:21787680
RGD:8695948
NCBI chr12:73,948,186...73,994,304
Ensembl chr12:73,948,149...73,994,304
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Hspa1a
heat shock protein 1A
ISO
DNA:SNP, haplotype: :rs1043618 (human)
RGD
PMID:17009596
RGD:8662466
NCBI chr17:35,188,335...35,191,132
Ensembl chr17:35,188,166...35,191,132
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Hspa1b
heat shock protein 1B
ISO
DNA:SNP, haplotype: :rs1061581 (human)
RGD
PMID:18813331
RGD:8662841
NCBI chr17:35,175,405...35,178,214
Ensembl chr17:35,175,412...35,178,214
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Hspa1l
heat shock protein 1-like
ISO
DNA:SNP, haplotype: :rs2227956 (human)
RGD
PMID:17009596
RGD:8662466
NCBI chr17:35,191,679...35,198,204
Ensembl chr17:35,191,679...35,198,261
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Icam1
intercellular adhesion molecule 1
ISO
RGD
PMID:19213042
RGD:8547577
NCBI chr 9:20,927,236...20,940,110
Ensembl chr 9:20,927,281...20,940,113
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Igf1
insulin-like growth factor 1
ISO
RGD
PMID:16585854
RGD:8549455
NCBI chr10:87,694,127...87,772,909
Ensembl chr10:87,694,127...87,772,904
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Il6
interleukin 6
ISO
RGD
PMID:16429448
RGD:7829818
NCBI chr 5:30,218,112...30,224,973
Ensembl chr 5:30,218,112...30,224,979
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Kcne1
potassium voltage-gated channel, Isk-related subfamily, member 1
ISO
CTD Direct Evidence: marker/mechanism ClinVar Annotator: match by term: Noise induced hearing loss
CTD ClinVar
PMID:7828904 PMID:9445165 PMID:12402336 PMID:14661677 PMID:14760488 PMID:15599693 PMID:16487223 PMID:16823764 PMID:17161064 PMID:17210839 PMID:17597962 PMID:18426444 PMID:22581653 PMID:23861362 PMID:24033266 PMID:25741868 PMID:28492532 More...
NCBI chr16:92,142,889...92,156,356
Ensembl chr16:92,142,870...92,156,356
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Kcnq1
potassium voltage-gated channel, subfamily Q, member 1
ISO
CTD Direct Evidence: marker/mechanism
CTD
PMID:16823764
NCBI chr 7:142,660,614...142,980,787
Ensembl chr 7:142,660,099...142,980,779
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Kcnq4
potassium voltage-gated channel, subfamily Q, member 4
ISO
CTD Direct Evidence: marker/mechanism
CTD
PMID:16823764
NCBI chr 4:120,553,331...120,605,809
Ensembl chr 4:120,553,335...120,605,809
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Mir107
microRNA 107
ISO
CTD Direct Evidence: marker/mechanism
CTD
PMID:23472202
NCBI chr19:34,798,087...34,798,173
Ensembl chr19:34,798,087...34,798,173
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Mir10a
microRNA 10a
ISO
CTD Direct Evidence: marker/mechanism
CTD
PMID:23472202
NCBI chr11:96,207,991...96,208,100
Ensembl chr11:96,207,991...96,208,100
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Mir130b
microRNA 130b
ISO
CTD Direct Evidence: marker/mechanism
CTD
PMID:23472202
NCBI chr16:16,941,925...16,942,006
Ensembl chr16:16,941,925...16,942,006
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Mir146b
microRNA 146b
ISO
CTD Direct Evidence: marker/mechanism
CTD
PMID:23472202
NCBI chr19:46,331,201...46,331,309
Ensembl chr19:46,331,201...46,331,309
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Mir183
microRNA 183
ISO
CTD Direct Evidence: marker/mechanism
CTD
PMID:23472202
NCBI chr 6:30,169,667...30,169,736
Ensembl chr 6:30,169,667...30,169,736
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Mir186
microRNA 186
ISO
CTD Direct Evidence: marker/mechanism
CTD
PMID:23472202
NCBI chr 3:157,249,916...157,249,986
Ensembl chr 3:157,249,916...157,249,986
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Mir190b
microRNA 190b
ISO
CTD Direct Evidence: marker/mechanism
CTD
PMID:23472202
NCBI chr 3:89,977,327...89,977,406
Ensembl chr 3:89,977,327...89,977,406
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Mir200c
microRNA 200c
ISO
CTD Direct Evidence: marker/mechanism
CTD
PMID:23472202
NCBI chr 6:124,695,285...124,695,353
Ensembl chr 6:124,695,285...124,695,353
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Mir30d
microRNA 30d
ISO
CTD Direct Evidence: marker/mechanism
CTD
PMID:23472202
NCBI chr15:68,213,057...68,213,138
Ensembl chr15:68,213,057...68,213,138
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Mir30e
microRNA 30e
ISO
CTD Direct Evidence: marker/mechanism
CTD
PMID:23472202
NCBI chr 4:120,629,803...120,629,894
Ensembl chr 4:120,629,803...120,629,894
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Mir325
microRNA 325
ISO
CTD Direct Evidence: marker/mechanism
CTD
PMID:23472202
NCBI chr X:104,422,688...104,422,785
Ensembl chr X:104,422,688...104,422,785
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Mir331
microRNA 331
ISO
CTD Direct Evidence: marker/mechanism
CTD
PMID:23472202
NCBI chr10:93,799,630...93,799,725
Ensembl chr10:93,799,630...93,799,725
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Mir339
microRNA 339
ISO
CTD Direct Evidence: marker/mechanism
CTD
PMID:23472202
NCBI chr 5:139,355,405...139,355,500
Ensembl chr 5:139,355,405...139,355,500
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Mir381
microRNA 381
ISO
CTD Direct Evidence: marker/mechanism
CTD
PMID:23472202
NCBI chr12:109,693,256...109,693,330
Ensembl chr12:109,693,256...109,693,330
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Mir429
microRNA 429
ISO
CTD Direct Evidence: marker/mechanism
CTD
PMID:23472202
NCBI chr 4:156,138,362...156,138,444
Ensembl chr 4:156,138,362...156,138,444
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Mir532
microRNA 532
ISO
CTD Direct Evidence: marker/mechanism
CTD
PMID:23472202
NCBI chr X:7,114,641...7,114,736
Ensembl chr X:7,114,641...7,114,736
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Mir674
microRNA 674
EXP
CTD Direct Evidence: marker/mechanism
CTD
PMID:23472202
NCBI chr 2:117,015,608...117,015,707
Ensembl chr 2:117,015,608...117,015,707
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Mir99b
microRNA 99b
ISO
CTD Direct Evidence: marker/mechanism
CTD
PMID:23472202
NCBI chr17:18,050,450...18,050,519
Ensembl chr17:18,050,450...18,050,519
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Mmp7
matrix metallopeptidase 7
IMP
RGD
PMID:23100416
RGD:9685340
NCBI chr 9:7,692,095...7,699,587
Ensembl chr 9:7,692,091...7,699,587
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Nob1
NIN1/RPN12 binding protein 1 homolog
ISO
mRNA:increased expression:cochlea
RGD
PMID:21219967
RGD:10766449
NCBI chr 8:108,139,121...108,151,670
Ensembl chr 8:108,139,118...108,151,683
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Nr3c1
nuclear receptor subfamily 3, group C, member 1
ISO
protein:increased expression:hippocampus
RGD
PMID:31071644
RGD:408364986
NCBI chr18:39,543,598...39,652,485
Ensembl chr18:39,543,598...39,652,474
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Ogg1
8-oxoguanine DNA-glycosylase 1
susceptibility
ISO
DNA:missense mutation:exon:p.S326C (rs1052133) (human) CTD Direct Evidence: marker/mechanism
CTD RGD
PMID:24599382 PMID:24599382
RGD:8657374
NCBI chr 6:113,303,959...113,311,149
Ensembl chr 6:113,303,933...113,312,029
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Pon2
paraoxonase 2
susceptibility
ISO
DNA:SNPs: :multiple
RGD
PMID:23327886
RGD:8661240
NCBI chr 6:5,264,620...5,298,408
Ensembl chr 6:5,264,147...5,298,455
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Proc
protein C
treatment
ISO
RGD
PMID:25108045
RGD:11100045
NCBI chr18:32,256,179...32,272,623
Ensembl chr18:32,256,179...32,272,623
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Ptger4
prostaglandin E receptor 4 (subtype EP4)
resistance
IMP
RGD
PMID:22198478
RGD:6483524
NCBI chr15:5,262,880...5,273,668
Ensembl chr15:5,236,142...5,273,668
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Sell
selectin, lymphocyte
ISO
RGD
PMID:22044737
RGD:5685697
NCBI chr 1:163,889,556...163,908,354
Ensembl chr 1:163,889,551...163,911,750
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Slc26a5
solute carrier family 26, member 5
IEP
mRNA, protein:increased expression:cochlea (mouse)
RGD
PMID:24376553
RGD:9585684
NCBI chr 5:22,013,999...22,070,602
Ensembl chr 5:22,015,653...22,070,602
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Sod1
superoxide dismutase 1, soluble
susceptibility severity
ISO IMP
DNA:snps, haplotypes:introns:multiple (human) DNA:snps:introns:IVS2+193T>G (rs10432782), IVS3-251A>G (rs2070424) (human)
RGD
PMID:19895330 PMID:22931816 PMID:10436316
RGD:8655611 , RGD:8655851 , RGD:8655966
NCBI chr16:90,017,650...90,023,221
Ensembl chr16:90,017,642...90,023,217
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Sod2
superoxide dismutase 2, mitochondrial
susceptibility
ISO
DNA:polymorphisms:intron:IVS3-23T>G, IVS3-60T>G (human) DNA:SNP:cds:p.V16A(rs4880)(human)
RGD
PMID:15345661 PMID:20534900
RGD:8158044 , RGD:8158046
NCBI chr17:13,226,726...13,237,006
Ensembl chr17:13,225,733...13,258,950
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Src
Rous sarcoma oncogene
treatment
ISO
RGD
PMID:21840347
RGD:11554196
NCBI chr 2:157,265,828...157,313,758
Ensembl chr 2:157,260,364...157,313,782
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Taok1
TAO kinase 1
ISO
CTD Direct Evidence: marker/mechanism
CTD
PMID:23472202
NCBI chr11:77,419,988...77,516,185
Ensembl chr11:77,419,988...77,498,641
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Tnf
tumor necrosis factor
ISO
mRNA:increased expression:cochlea:
RGD
PMID:19051071
RGD:7394705
NCBI chr17:35,418,343...35,420,983
Ensembl chr17:35,418,357...35,420,983
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