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RGD DISEASE ONTOLOGY - ANNOTATIONS

RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) 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:mixed glioma
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Accession:DOID:5076 term browser browse the term
Synonyms:exact_synonym: mixed gliomas;   mixed neuroglial tumor
 xref: NCI:C3903
For additional species annotation, visit the Alliance of Genome Resources.

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mixed glioma term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G N Rtel1 regulator of telomere elongation helicase 1 susceptibility ISO DNA:SNPs:multiple:multiple (human) RGD PMID:30462709 RGD:152977767 NCBI chrNW_004624741:29,303,844...29,344,123
Ensembl chrNW_004624741:29,304,427...29,343,842 		JBrowse link
G G RTEL1 regulator of telomere elongation helicase 1 susceptibility ISO DNA:SNPs:multiple:multiple (human) RGD PMID:30462709 RGD:152977767 NCBI chr 2:531,905...567,430
Ensembl chr 2:531,085...566,840 		JBrowse link
G P RTEL1 regulator of telomere elongation helicase 1 susceptibility ISO DNA:SNPs:multiple:multiple (human) RGD PMID:30462709 RGD:152977767 NCBI chr17:62,611,844...62,636,628
Ensembl chr17:62,611,909...62,634,690 		JBrowse link
G S Rtel1 regulator of telomere elongation helicase 1 susceptibility ISO DNA:SNPs:multiple:multiple (human) RGD PMID:30462709 RGD:152977767 NCBI chrNW_004936514:10,920,979...10,954,483
Ensembl chrNW_004936514:10,922,322...10,954,402 		JBrowse link
G D RTEL1 regulator of telomere elongation helicase 1 susceptibility ISO DNA:SNPs:multiple:multiple (human) RGD PMID:30462709 RGD:152977767 NCBI chr24:47,219,977...47,248,791 JBrowse link
G B RTEL1 regulator of telomere elongation helicase 1 susceptibility ISO DNA:SNPs:multiple:multiple (human) RGD PMID:30462709 RGD:152977767 Ensembl chr20:61,581,331...61,618,718 JBrowse link
G C Rtel1 regulator of telomere elongation helicase 1 susceptibility ISO DNA:SNPs:multiple:multiple (human) RGD PMID:30462709 RGD:152977767 NCBI chrNW_004955528:531,680...578,003
Ensembl chrNW_004955528:532,385...572,398 		JBrowse link
G R Rtel1 regulator of telomere elongation helicase 1 susceptibility ISO DNA:SNPs:multiple:multiple (human) RGD PMID:30462709 RGD:152977767 NCBI chr 3:168,427,247...168,465,349
Ensembl chr 3:168,419,579...168,465,348 		JBrowse link
G M Rtel1 regulator of telomere elongation helicase 1 susceptibility ISO DNA:SNPs:multiple:multiple (human) RGD PMID:30462709 RGD:152977767 NCBI chr 2:180,961,504...180,998,409
Ensembl chr 2:180,961,532...180,998,409 		JBrowse link
G H RTEL1 regulator of telomere elongation helicase 1 susceptibility IAGP DNA:SNPs:multiple:multiple (human) RGD PMID:30462709 RGD:152977767 NCBI chr20:63,657,810...63,696,253
Ensembl chr20:63,657,810...63,696,253 		JBrowse link
Term paths to the root
Path 1
Term Annotations click to browse term
  disease 199759
    disease of cellular proliferation 73774
      cancer 75316
        cell type cancer 36265
          high grade glioma 7016
            mixed glioma 10
              mixed astrocytoma-ependymoma 0
              mixed astrocytoma-ependymoma-oligodendroglioma 0
              mixed oligodendroglioma-astrocytoma 0
Path 2
Term Annotations click to browse term
  disease 199759
    disease of anatomical entity 167983
      nervous system disease 142629
        central nervous system disease 127613
          Central Nervous System Neoplasms 14128
            Brain Neoplasms 13653
              brain cancer 7587
                high grade glioma 7016
                  mixed glioma 10
                    mixed astrocytoma-ependymoma 0
                    mixed astrocytoma-ependymoma-oligodendroglioma 0
                    mixed oligodendroglioma-astrocytoma 0
paths to the root