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RGD uses the Human Disease Ontology (DO, for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.

Term:retinitis pigmentosa 1
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Accession:DOID:0110390 term browser browse the term
Definition:A retinitis pigmentosa that has_material_basis_in mutation in the RP1 gene on chromosome 8q12. (DO)
Synonyms:exact_synonym: RP1
 primary_id: MESH:C538365
 alt_id: OMIM:180100
For additional species annotation, visit the Alliance of Genome Resources.

show annotations for term's descendants           Sort by:
retinitis pigmentosa 1 term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Rp1 RP1, axonemal microtubule associated ISO ClinVar Annotator: match by OMIM:180100
ClinVar Annotator: match by null
ClinVar Annotator: match by term: Retinitis pigmentosa 1
PMID:1783394, PMID:8931712, PMID:10391211, PMID:10391212, PMID:10401003, PMID:10465120, PMID:10845615, PMID:11527933, PMID:15863674, PMID:15994872, PMID:19933189, PMID:21147909, PMID:24265693, PMID:25741868, PMID:28041643, PMID:28492532, PMID:29425069, PMID:29847639, PMID:30027431, PMID:30718709 NCBI chr 5:15,005,028...15,060,508
Ensembl chr 5:15,043,955...15,060,508
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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16045
    sensory system disease 5213
      eye disease 2652
        Hereditary Eye Diseases 576
          retinitis pigmentosa 266
            retinitis pigmentosa 1 1
Path 2
Term Annotations click to browse term
  disease 16045
    disease of anatomical entity 15292
      nervous system disease 10879
        sensory system disease 5213
          eye disease 2652
            retinal disease 780
              retinal degeneration 466
                fundus dystrophy 333
                  retinitis pigmentosa 266
                    retinitis pigmentosa 1 1
paths to the root


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