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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: Autosomal dominant nonsyndromic hereditary hearing impairment;   Deafness, nonsyndromic sensorineural, mitochondrial;   Nonsyndromic hearing loss, dominant;   Nonsyndromic hereditary hearing impairment
 primary_id: MESH:C537845;   RDO:0003755
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Nonsyndromic Sensorineural Hearing Loss term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Coch cochlin JBrowse link 6 72,359,702 72,373,710 RGD:8554872
G Col11a2 collagen type XI alpha 2 chain JBrowse link 20 3,829,324 3,859,022 RGD:8554872
G Eya4 EYA transcriptional coactivator and phosphatase 4 JBrowse link 1 23,237,617 23,611,580 RGD:8554872
G Gja1 gap junction protein, alpha 1 JBrowse link 20 37,876,650 37,889,097 RGD:1578475
G Gjb2 gap junction protein, beta 2 JBrowse link 15 37,377,313 37,394,494 RGD:7364796
RGD:8554872
RGD:7364798
RGD:7364803
RGD:7364812
RGD:7364817
RGD:7364823
RGD:7364883
RGD:7364888
RGD:7364892
G Gjb3 gap junction protein, beta 3 JBrowse link 5 145,390,590 145,397,271 RGD:1300214
RGD:8554872
RGD:12050154
RGD:7364900
G Gjb6 gap junction protein, beta 6 JBrowse link 15 37,400,888 37,411,656 RGD:7364803
RGD:8554872
RGD:7364892
RGD:7364891
RGD:7364817
RGD:7364812
G Mt-co1 mitochondrially encoded cytochrome c oxidase I JBrowse link MT 5,323 6,867 RGD:8554872
G Mt-nd1 mitochondrially encoded NADH dehydrogenase 1 JBrowse link MT 2,740 3,694 RGD:8554872
G Myh14 myosin heavy chain 14 JBrowse link 1 100,608,975 100,671,086 RGD:8554872
G Myh9 myosin, heavy chain 9 JBrowse link 7 118,740,005 118,792,507 RGD:11533925
RGD:8554872
G Myo1a myosin IA JBrowse link 7 71,000,299 71,019,386 RGD:8554872
G Myo6 myosin VI JBrowse link 8 87,583,649 87,731,271 RGD:8554872
G Myo7a myosin VIIA JBrowse link 1 163,001,313 163,071,545 RGD:8554872
G Pnpt1 polyribonucleotide nucleotidyltransferase 1 JBrowse link 14 113,530,470 113,561,645 RGD:11554169
G Pou4f3 POU class 4 homeobox 3 JBrowse link 18 36,713,869 36,716,461 RGD:8554872
G Six1 SIX homeobox 1 JBrowse link 6 95,929,060 95,934,296 RGD:8554872
G Slc17a8 solute carrier family 17 member 8 JBrowse link 7 30,215,231 30,274,993 RGD:8554872
G Slc26a5 solute carrier family 26 member 5 JBrowse link 4 9,795,811 9,860,904 RGD:7364803
G Tecta tectorin alpha JBrowse link 8 46,603,728 46,675,658 RGD:8554872
G Tjp2 tight junction protein 2 JBrowse link 1 241,945,816 242,084,044 RGD:8554872
G Tmc1 transmembrane channel-like 1 JBrowse link 1 238,336,919 238,525,792 RGD:8554872
G Tmtc2 transmembrane O-mannosyltransferase targeting cadherins 2 JBrowse link 7 47,179,596 47,586,777 RGD:11252147
G Wfs1 wolframin ER transmembrane glycoprotein JBrowse link 14 78,640,707 78,665,224 RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15620
    sensory system disease 4681
      auditory system disease 684
        inner ear disease 495
          sensorineural hearing loss 459
            Nonsyndromic Sensorineural Hearing Loss 24
Path 2
Term Annotations click to browse term
  disease 15620
    disease of anatomical entity 14949
      nervous system disease 10219
        sensory system disease 4681
          Otorhinolaryngologic Diseases 1075
            auditory system disease 684
              Hearing Disorders 569
                Hearing Loss 565
                  sensorineural hearing loss 459
                    Nonsyndromic Sensorineural Hearing Loss 24
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.