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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 7 68,580,124 68,595,142 RGD:9068941
G COL11A2 collagen type XI alpha 2 chain JBrowse link 7 25,204,496 25,234,880 RGD:9068941
G EYA4 EYA transcriptional coactivator and phosphatase 4 JBrowse link 1 30,260,784 30,575,593 RGD:9068941
G GJA1 gap junction protein alpha 1 JBrowse link 1 40,988,818 41,002,129 RGD:9068941
G GJB2 gap junction protein beta 2 JBrowse link 11 774,090 781,252 RGD:9068941
G GJB3 gap junction protein beta 3 JBrowse link 6 91,031,378 91,037,548 RGD:9068941
G GJB6 gap junction protein beta 6 JBrowse link 11 793,276 800,109 RGD:9068941
G LOC100523684 tubulin-specific chaperone cofactor E-like protein JBrowse link 9 48,120,786 48,286,275 RGD:9068941
G MYH14 myosin heavy chain 14 JBrowse link 6 55,097,851 55,200,754 RGD:9068941
G MYH9 myosin heavy chain 9 JBrowse link 5 11,365,603 11,456,475 RGD:9068941
G MYO1A myosin IA JBrowse link 5 22,338,024 22,363,528 RGD:9068941
G MYO6 myosin VI JBrowse link 1 89,992,860 90,137,767 RGD:9068941
G MYO7A myosin VIIA JBrowse link 9 11,251,187 11,337,618 RGD:9068941
G PNPT1 polyribonucleotide nucleotidyltransferase 1 JBrowse link 3 85,595,356 85,639,665 RGD:9068941
G POU4F3 POU class 4 homeobox 3 JBrowse link 2 147,693,013 147,694,345 RGD:9068941
G SIX1 SIX homeobox 1 JBrowse link 1 189,620,430 189,624,652 RGD:9068941
G SLC17A8 solute carrier family 17 member 8 JBrowse link 5 83,741,641 83,809,472 RGD:9068941
G SLC26A5 solute carrier family 26 member 5 JBrowse link 9 103,382,558 103,420,054 RGD:9068941
G TJP2 tight junction protein 2 JBrowse link 1 222,474,518 222,612,989 RGD:9068941
G TMC1 transmembrane channel like 1 JBrowse link 1 225,714,601 226,111,045 RGD:9068941
G TMTC2 transmembrane O-mannosyltransferase targeting cadherins 2 JBrowse link 5 98,695,404 99,085,243 RGD:9068941
G WFS1 wolframin ER transmembrane glycoprotein JBrowse link 8 4,362,678 4,405,185 RGD:9068941
mitochondrial nonsyndromic sensorineural deafness term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G MT-CO1 mitochondrially encoded cytochrome c oxidase I JBrowse link MT 6,511 8,055 RGD:9068941
G MT-ND1 mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 JBrowse link MT 3,922 4,876 RGD:9068941

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 12518
    sensory system disease 4535
      auditory system disease 650
        inner ear disease 462
          sensorineural hearing loss 424
            Nonsyndromic Sensorineural Hearing Loss 24
              mitochondrial nonsyndromic sensorineural deafness 2
Path 2
Term Annotations click to browse term
  disease 12518
    disease of anatomical entity 12073
      nervous system disease 9798
        sensory system disease 4535
          Otorhinolaryngologic Diseases 1039
            auditory system disease 650
              Hearing Disorders 529
                Hearing Loss 525
                  sensorineural hearing loss 424
                    Nonsyndromic Sensorineural Hearing Loss 24
                      mitochondrial nonsyndromic sensorineural deafness 2
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.