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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:UV-Sensitive Syndrome 1
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Accession:DOID:9006274 term browser browse the term
Synonyms:exact_synonym: UVSS1
 primary_id: OMIM:600630
 alt_id: RDO:0008765
 xref: NCI:C173106
For additional species annotation, visit the Alliance of Genome Resources.

show annotations for term's descendants           Sort by:
UV-Sensitive Syndrome 1 term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Ercc6 ERCC excision repair 6, chromatin remodeling factor ISO ClinVar Annotator: match by term: UV-sensitive syndrome 1
ClinVar Annotator: match by term: UV-SENSITIVE SYNDROME 1
PMID:7264357 PMID:9443879 PMID:9777763 PMID:10767341 PMID:15486090 More... NCBI chr16:7,764,983...7,835,587
Ensembl chr16:7,765,013...7,835,587
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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 17289
    syndrome 8166
      UV-sensitive syndrome 3
        UV-Sensitive Syndrome 1 1
Path 2
Term Annotations click to browse term
  disease 17289
    Developmental Disease 10990
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9530
        genetic disease 9033
          monogenic disease 7190
            autosomal genetic disease 6337
              autosomal recessive disease 3496
                UV-sensitive syndrome 3
                  UV-Sensitive Syndrome 1 1
paths to the root