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ONTOLOGY REPORT - ANNOTATIONS


Term:Nonsyndromic Sensorineural Hearing Loss
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Accession:DOID:9007966 term browser browse the term
Synonyms:exact_synonym: Nonsyndromic hearing loss, dominant;   autosomal dominant nonsyndromic hereditary hearing impairment;   nonsyndromic hereditary hearing impairment
 primary_id: MESH:C537845
For additional species annotation, visit the Alliance of Genome Resources.


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Nonsyndromic Sensorineural Hearing Loss term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Coch cochlin JBrowse link 12 51,593,283 51,606,619 RGD:8554872
G Col11a2 collagen, type XI, alpha 2 JBrowse link 17 34,038,919 34,066,684 RGD:8554872
G Eya4 EYA transcriptional coactivator and phosphatase 4 JBrowse link 10 23,102,962 23,350,838 RGD:8554872
G Gja1 gap junction protein, alpha 1 JBrowse link 10 56,377,300 56,390,419 RGD:1578475
G Gjb2 gap junction protein, beta 2 JBrowse link 14 57,098,602 57,104,702 RGD:7364796
RGD:8554872
RGD:7364892
RGD:7364888
RGD:7364883
RGD:7364823
RGD:7364817
RGD:7364812
RGD:7364798
RGD:7364803
G Gjb3 gap junction protein, beta 3 JBrowse link 4 127,325,235 127,330,836 RGD:1300214
RGD:8554872
RGD:12050154
RGD:7364900
G Gjb6 gap junction protein, beta 6 JBrowse link 14 57,123,301 57,133,611 RGD:7364803
RGD:8554872
RGD:7364812
RGD:7364817
RGD:7364891
RGD:7364892
G Myh14 myosin, heavy polypeptide 14 JBrowse link 7 44,605,803 44,670,872 RGD:8554872
G Myh9 myosin, heavy polypeptide 9, non-muscle JBrowse link 15 77,760,585 77,842,175 RGD:11533925
RGD:8554872
G Myo1a myosin IA JBrowse link 10 127,703,436 127,720,940 RGD:8554872
G Myo6 myosin VI JBrowse link 9 80,164,976 80,311,729 RGD:8554872
G Myo7a myosin VIIA JBrowse link 7 98,051,054 98,119,522 RGD:8554872
G Pnpt1 polyribonucleotide nucleotidyltransferase 1 JBrowse link 11 29,130,129 29,161,827 RGD:11554169
G Pou4f3 POU domain, class 4, transcription factor 3 JBrowse link 18 42,394,597 42,396,093 RGD:8554872
G Six1 sine oculis-related homeobox 1 JBrowse link 12 73,041,827 73,046,712 RGD:8554872
G Slc17a8 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8 JBrowse link 10 89,574,020 89,621,249 RGD:8554872
G Slc26a5 solute carrier family 26, member 5 JBrowse link 5 21,809,001 21,865,604 RGD:7364803
G Tecta tectorin alpha JBrowse link 9 42,329,622 42,401,690 RGD:8554872
G Tjp2 tight junction protein 2 JBrowse link 19 24,094,496 24,225,128 RGD:8554872
G Tmc1 transmembrane channel-like gene family 1 JBrowse link 19 20,783,456 21,037,126 RGD:8554872
G Tmtc2 transmembrane and tetratricopeptide repeat containing 2 JBrowse link 10 105,187,663 105,574,479 RGD:11252147
G Wfs1 wolframin ER transmembrane glycoprotein JBrowse link 5 36,966,104 36,988,982 RGD:8554872
mitochondrial nonsyndromic sensorineural deafness term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G mt-Co1 cytochrome c oxidase I, mitochondrial JBrowse link MT 5,328 6,872 RGD:8554872
RGD:13592920
G mt-Nd1 NADH dehydrogenase 1, mitochondrial JBrowse link MT 2,751 3,707 RGD:8554872
G mt-Rnr1 12S rRNA, mitochondrial JBrowse link MT 70 1,024 RGD:8554872
RGD:13592920
G mt-Th tRNA histidine, mitochondrial JBrowse link MT 11,546 11,612 RGD:8554872
G mt-Ti tRNA isoleucine, mitochondrial JBrowse link MT 3,706 3,774 RGD:8554872
G mt-Ts1 tRNA serine 1, mitochondrial JBrowse link MT 6,870 6,938 RGD:8554872
RGD:13592920

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 13235
    sensory system disease 4776
      auditory system disease 704
        inner ear disease 498
          sensorineural hearing loss 459
            Nonsyndromic Sensorineural Hearing Loss 28
              mitochondrial nonsyndromic sensorineural deafness 6
Path 2
Term Annotations click to browse term
  disease 13235
    disease of anatomical entity 12738
      nervous system disease 10275
        sensory system disease 4776
          Otorhinolaryngologic Diseases 1114
            auditory system disease 704
              Hearing Disorders 567
                Hearing Loss 563
                  sensorineural hearing loss 459
                    Nonsyndromic Sensorineural Hearing Loss 28
                      mitochondrial nonsyndromic sensorineural deafness 6
paths to the root

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.