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ONTOLOGY REPORT - ANNOTATIONS


Term:retinitis pigmentosa 77
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Accession:DOID:0080350 term browser browse the term
Definition:A retinitis pigmentosa that has_material_basis_in mutation in the REEP6 gene on chromosome 19p13. (DO)
Synonyms:exact_synonym: RP77
 primary_id: OMIM:617304
 alt_id: DOID:9004326;   RDO:9001540
For additional species annotation, visit the Alliance of Genome Resources.


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retinitis pigmentosa 77 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Reep6 receptor accessory protein 6 JBrowse link 7 12,240,059 12,246,814 RGD:8554872
RGD:7240710

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15619
    sensory system disease 4674
      eye and adnexa disease 2242
        eye disease 2242
          Hereditary Eye Diseases 507
            retinitis pigmentosa 242
              retinitis pigmentosa 77 1
Path 2
Term Annotations click to browse term
  disease 15619
    disease of anatomical entity 14948
      nervous system disease 10216
        sensory system disease 4674
          eye and adnexa disease 2242
            eye disease 2242
              retinal disease 715
                retinal degeneration 407
                  fundus dystrophy 264
                    retinitis pigmentosa 242
                      retinitis pigmentosa 77 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.