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ONTOLOGY REPORT - ANNOTATIONS


Term:night blindness
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Accession:DOID:8499 term browser browse the term
Definition:Failure or imperfection of vision at night or in dim light, with good vision only on bright days. (Dorland, 27th ed)
Synonyms:exact_synonym: Nyctalopia
 primary_id: MESH:D009755;   RDO:0001564
 xref: NCI:C34850;   NCI:C37997
For additional species annotation, visit the Alliance of Genome Resources.


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night blindness term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G CHM CHM Rab escort protein JBrowse link X 85,861,180 86,047,558 RGD:8554872
G GNAT1 G protein subunit alpha transducin 1 JBrowse link 3 50,191,610 50,197,696 RGD:1599006
G GRK1 G protein-coupled receptor kinase 1 JBrowse link 13 113,645,771 113,737,736 RGD:1600000
G NRL neural retina leucine zipper JBrowse link 14 24,078,686 24,114,949 RGD:11554173
G NYX nyctalopin JBrowse link X 41,447,460 41,476,414 RGD:1601021
G RDH5 retinol dehydrogenase 5 JBrowse link 12 55,720,393 55,724,742 RGD:1599416
G RHO rhodopsin JBrowse link 3 129,528,639 129,535,344 RGD:1601620
RGD:8554872
G RLBP1 retinaldehyde binding protein 1 JBrowse link 15 89,209,869 89,223,179 RGD:1599620
congenital stationary night blindness term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G ABCA4 ATP binding cassette subfamily A member 4 JBrowse link 1 93,992,834 94,121,148 RGD:8554872
G CABP4 calcium binding protein 4 JBrowse link 11 67,452,403 67,461,774 RGD:8554872
G CACNA1F calcium voltage-gated channel subunit alpha1 F JBrowse link X 49,205,063 49,233,404 RGD:734671
RGD:13782370
RGD:11554173
RGD:8554872
G DENND4A DENN domain containing 4A JBrowse link 15 65,655,234 65,792,293 RGD:8554872
G GNAT1 G protein subunit alpha transducin 1 JBrowse link 3 50,191,610 50,197,696 RGD:8554872
RGD:11554173
G GNB3 G protein subunit beta 3 JBrowse link 12 6,840,922 6,847,393 RGD:11554173
G GPR179 G protein-coupled receptor 179 JBrowse link 17 38,324,571 38,343,956 RGD:8554872
RGD:11554173
G GRK1 G protein-coupled receptor kinase 1 JBrowse link 13 113,645,771 113,737,736 RGD:8554872
G GRM6 glutamate metabotropic receptor 6 JBrowse link 5 178,978,327 178,995,320 RGD:8554872
RGD:11554173
G LRIT3 leucine rich repeat, Ig-like and transmembrane domains 3 JBrowse link 4 109,848,107 109,872,315 RGD:8554872
RGD:11554173
G NYX nyctalopin JBrowse link X 41,447,460 41,476,414 RGD:8554872
RGD:11554173
G PDE6B phosphodiesterase 6B JBrowse link 4 587,325 670,892 RGD:8554872
RGD:11554173
G PDE6B-AS1 PDE6B antisense RNA 1 JBrowse link 4 652,909 656,188 RGD:8554872
G RHO rhodopsin JBrowse link 3 129,528,639 129,535,344 RGD:8554872
RGD:11554173
G RPGR retinitis pigmentosa GTPase regulator JBrowse link X 38,269,163 38,327,509 RGD:8554872
G SAG S-antigen visual arrestin JBrowse link 2 233,307,816 233,347,066 RGD:11554173
G SLC24A1 solute carrier family 24 member 1 JBrowse link 15 65,611,313 65,661,002 RGD:8554872
RGD:11554173
G TRPM1 transient receptor potential cation channel subfamily M member 1 JBrowse link 15 31,001,061 31,161,273 RGD:7175555
RGD:8554872
RGD:11554173
RGD:7183085
RGD:7183084
G TRPV3 transient receptor potential cation channel subfamily V member 3 JBrowse link 17 3,510,502 3,557,812 RGD:7175555
G USH2A usherin JBrowse link 1 215,622,891 216,423,448 RGD:8554872
congenital stationary night blindness 1A term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G NYX nyctalopin JBrowse link X 41,447,460 41,476,414 RGD:8554872
RGD:7240710
congenital stationary night blindness 1B term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G GRM6 glutamate metabotropic receptor 6 JBrowse link 5 178,978,327 178,995,320 RGD:8554872
RGD:7240710
G SLC24A1 solute carrier family 24 member 1 JBrowse link 15 65,611,313 65,661,002 RGD:8554872
congenital stationary night blindness 1C term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G SLC24A1 solute carrier family 24 member 1 JBrowse link 15 65,611,313 65,661,002 RGD:8554872
G TRPM1 transient receptor potential cation channel subfamily M member 1 JBrowse link 15 31,001,061 31,161,273 RGD:8554872
RGD:7240710
congenital stationary night blindness 1D term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G SLC24A1 solute carrier family 24 member 1 JBrowse link 15 65,611,313 65,661,002 RGD:8554872
RGD:7240710
congenital stationary night blindness 1E term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G GPR179 G protein-coupled receptor 179 JBrowse link 17 38,324,571 38,343,956 RGD:8554872
RGD:7240710
G SLC24A1 solute carrier family 24 member 1 JBrowse link 15 65,611,313 65,661,002 RGD:8554872
congenital stationary night blindness 1F term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G LRIT3 leucine rich repeat, Ig-like and transmembrane domains 3 JBrowse link 4 109,848,107 109,872,315 RGD:8554872
RGD:7240710
congenital stationary night blindness 1G term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G GNAT1 G protein subunit alpha transducin 1 JBrowse link 3 50,191,610 50,197,696 RGD:7240710
RGD:8554872
congenital stationary night blindness 1H term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G CDCA3 cell division cycle associated 3 JBrowse link 12 6,844,795 6,852,079 RGD:8554872
G GNB3 G protein subunit beta 3 JBrowse link 12 6,840,922 6,847,393 RGD:8554872
RGD:7240710
Congenital Stationary Night Blindness 1I term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G GUCY2D guanylate cyclase 2D, retinal JBrowse link 17 8,002,615 8,020,342 RGD:7240710
RGD:8554872
congenital stationary night blindness 2A term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G CACNA1F calcium voltage-gated channel subunit alpha1 F JBrowse link X 49,205,063 49,233,404 RGD:8554872
RGD:7240710
Congenital Stationary Night Blindness 2B term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G CABP4 calcium binding protein 4 JBrowse link 11 67,452,403 67,461,774 RGD:8554872
RGD:7240710
congenital stationary night blindness autosomal dominant 1 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G RHO rhodopsin JBrowse link 3 129,528,639 129,535,344 RGD:8554872
RGD:7240710
congenital stationary night blindness autosomal dominant 2 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G PDE6B phosphodiesterase 6B JBrowse link 4 587,325 670,892 RGD:8554872
RGD:7240710
G PDE6B-AS1 PDE6B antisense RNA 1 JBrowse link 4 652,909 656,188 RGD:8554872
congenital stationary night blindness autosomal dominant 3 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G GNAT1 G protein subunit alpha transducin 1 JBrowse link 3 50,191,610 50,197,696 RGD:8554872
RGD:7240710
Duchenne Muscular Dystrophy, Mental Retardation, and Absence of ERG B-wave term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G DMD dystrophin JBrowse link X 31,119,219 33,339,460 RGD:8554872
hereditary night blindness term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G GRK1 G protein-coupled receptor kinase 1 JBrowse link 13 113,645,771 113,737,736 RGD:11554173
RGD:8554872
G SAG S-antigen visual arrestin JBrowse link 2 233,307,816 233,347,066 RGD:734491
RGD:8554872
RGD:11554173
Oguchi disease-1 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G SAG S-antigen visual arrestin JBrowse link 2 233,307,816 233,347,066 RGD:7240710
RGD:8554872
Oguchi disease-2 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G GRK1 G protein-coupled receptor kinase 1 JBrowse link 13 113,645,771 113,737,736 RGD:8554872
RGD:7240710

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16432
    sensory system disease 4887
      eye and adnexa disease 2400
        eye disease 2400
          retinal disease 836
            night blindness 27
              Duchenne Muscular Dystrophy, Mental Retardation, and Absence of ERG B-wave 1
              Fleck Retina of Kandori 0
              Night Blindness Skeletal Anomalies Unusual Facies 0
              abnormal threshold of rods 0
              dominant pericentral pigmentary retinopathy 0
              hereditary night blindness + 22
Path 2
Term Annotations click to browse term
  disease 16432
    disease of anatomical entity 15407
      nervous system disease 11675
        sensory system disease 4887
          eye and adnexa disease 2400
            eye disease 2400
              retinal disease 836
                night blindness 27
                  Duchenne Muscular Dystrophy, Mental Retardation, and Absence of ERG B-wave 1
                  Fleck Retina of Kandori 0
                  Night Blindness Skeletal Anomalies Unusual Facies 0
                  abnormal threshold of rods 0
                  dominant pericentral pigmentary retinopathy 0
                  hereditary night blindness + 22
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.