Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

ONTOLOGY REPORT - ANNOTATIONS


Term:Nonsyndromic Sensorineural Hearing Loss
go back to main search page
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.


show annotations for term's descendants       view all columns           Sort by:
 
Nonsyndromic Sensorineural Hearing Loss term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G COCH cochlin JBrowse link 8 10,215,101 10,230,017 RGD:9068941
G COL11A2 collagen type XI alpha 2 chain JBrowse link 12 2,626,829 2,656,680 RGD:9068941
G EYA4 EYA transcriptional coactivator and phosphatase 4 JBrowse link 1 26,208,514 26,514,601 RGD:9068941
G GJA1 gap junction protein alpha 1 JBrowse link 1 60,941,772 60,944,694 RGD:9068941
G GJB2 gap junction protein beta 2 JBrowse link 25 17,952,851 17,958,289 RGD:9068941
G GJB3 gap junction protein beta 3 JBrowse link 15 7,175,010 7,177,145 RGD:9068941
G GJB6 gap junction protein beta 6 JBrowse link 25 17,912,036 17,922,310 RGD:9068941
G MYH14 myosin heavy chain 14 JBrowse link 1 106,371,952 106,460,388 RGD:9068941
G MYH9 myosin heavy chain 9 JBrowse link 10 28,063,626 28,122,953 RGD:9068941
G MYO1A myosin IA JBrowse link 10 1,159,816 1,194,452 RGD:9068941
G MYO6 myosin VI JBrowse link 12 37,359,200 37,502,342 RGD:9068941
G MYO7A myosin VIIA JBrowse link 21 21,539,735 21,624,063 RGD:9068941
G PNPT1 polyribonucleotide nucleotidyltransferase 1 JBrowse link 10 56,478,771 56,520,992 RGD:9068941
G POU4F3 POU class 4 homeobox 3 JBrowse link 2 40,762,499 40,764,131 RGD:9068941
G SIX1 SIX homeobox 1 JBrowse link 8 35,676,705 35,679,534 RGD:9068941
G SLC17A8 solute carrier family 17 member 8 JBrowse link 15 39,443,790 39,489,988 RGD:9068941
G SLC26A5 solute carrier family 26 member 5 JBrowse link 18 16,783,795 16,841,946 RGD:9068941
G TECTA tectorin alpha JBrowse link 5 12,879,963 12,949,211 RGD:9068941
G TJP2 tight junction protein 2 JBrowse link 1 88,126,134 88,251,018 RGD:9068941
G TMC1 transmembrane channel like 1 JBrowse link 1 85,041,039 85,159,607 RGD:9068941
G TMTC2 transmembrane O-mannosyltransferase targeting cadherins 2 JBrowse link 15 24,629,610 25,017,936 RGD:9068941
G WFS1 wolframin ER transmembrane glycoprotein JBrowse link 13 38,451,722 38,466,481 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 5,349 6,893 RGD:9068941
G MT-ND1 mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 JBrowse link MT 2,747 3,702 RGD:9068941

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 12601
    sensory system disease 4576
      auditory system disease 650
        inner ear disease 466
          sensorineural hearing loss 427
            Nonsyndromic Sensorineural Hearing Loss 24
              mitochondrial nonsyndromic sensorineural deafness 2
Path 2
Term Annotations click to browse term
  disease 12601
    disease of anatomical entity 12145
      nervous system disease 9867
        sensory system disease 4576
          Otorhinolaryngologic Diseases 1036
            auditory system disease 650
              Hearing Disorders 529
                Hearing Loss 525
                  sensorineural hearing loss 427
                    Nonsyndromic Sensorineural Hearing Loss 24
                      mitochondrial nonsyndromic sensorineural deafness 2
paths to the root

NHLBI Logo

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