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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
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Nonsyndromic Sensorineural Hearing Loss term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Coch cochlin JBrowse link NW_004936494 5,617,201 5,633,500 RGD:9068941
G Col11a2 collagen type XI alpha 2 chain JBrowse link NW_004936476 25,663,563 25,692,315 RGD:9068941
G Eya4 EYA transcriptional coactivator and phosphatase 4 JBrowse link NW_004936560 1,325,521 1,466,216 RGD:9068941
G Gjb2 gap junction protein beta 2 JBrowse link NW_004936720 1,528,205 1,530,296 RGD:9068941
G Gjb3 gap junction protein beta 3 JBrowse link NW_004936474 17,427,255 17,431,368 RGD:9068941
G Gjb6 gap junction protein beta 6 JBrowse link NW_004936720 1,485,895 1,494,673 RGD:9068941
G Myh14 myosin heavy chain 14 JBrowse link NW_004936889 121,724 184,374 RGD:9068941
G Myh9 myosin heavy chain 9 JBrowse link NW_004936492 4,384,215 4,466,229 RGD:9068941
G Myo1a myosin IA JBrowse link NW_004936646 1,238,630 1,258,491 RGD:9068941
G Myo6 myosin VI JBrowse link NW_004936788 1,125,332 1,264,372 RGD:9068941
G Myo7a myosin VIIA JBrowse link NW_004936498 5,758,572 5,824,526 RGD:9068941
G Pnpt1 polyribonucleotide nucleotidyltransferase 1 JBrowse link NW_004936491 1,989,429 2,032,430 RGD:9068941
G Pou4f3 POU class 4 homeobox 3 JBrowse link NW_004936504 8,348,460 8,351,246 RGD:9068941
G Six1 SIX homeobox 1 JBrowse link NW_004936495 4,839,496 4,842,906 RGD:9068941
G Slc17a8 solute carrier family 17 member 8 JBrowse link NW_004936492 13,436,136 13,486,173 RGD:9068941
G Slc26a5 solute carrier family 26 member 5 JBrowse link NW_004936479 20,104,625 20,145,392 RGD:9068941
G Tecta tectorin alpha JBrowse link NW_004936542 5,884,624 5,951,260 RGD:9068941
G Tjp2 tight junction protein 2 JBrowse link NW_004936503 5,414,330 5,539,895 RGD:9068941
G Tmc1 transmembrane channel like 1 JBrowse link NW_004936503 8,669,465 8,826,340 RGD:9068941
G Tmtc2 transmembrane O-mannosyltransferase targeting cadherins 2 JBrowse link NW_004936507 603,222 980,229 RGD:9068941
G Wfs1 wolframin ER transmembrane glycoprotein JBrowse link NW_004936477 18,339,915 18,364,973 RGD:9068941

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 11848
    sensory system disease 4374
      auditory system disease 617
        inner ear disease 437
          sensorineural hearing loss 400
            Nonsyndromic Sensorineural Hearing Loss 21
              mitochondrial nonsyndromic sensorineural deafness 0
Path 2
Term Annotations click to browse term
  disease 11848
    disease of anatomical entity 11432
      nervous system disease 9321
        sensory system disease 4374
          Otorhinolaryngologic Diseases 992
            auditory system disease 617
              Hearing Disorders 501
                Hearing Loss 497
                  sensorineural hearing loss 400
                    Nonsyndromic Sensorineural Hearing Loss 21
                      mitochondrial nonsyndromic sensorineural deafness 0
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.