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ONTOLOGY REPORT - ANNOTATIONS


Term:Mitochondrial Complex I Deficiency, Nuclear Type 21
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Accession:DOID:9009271 term browser browse the term
Synonyms:exact_synonym: MC1DN21
 primary_id: OMIM:618242
For additional species annotation, visit the Alliance of Genome Resources.


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Mitochondrial Complex I Deficiency, Nuclear Type 21 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Dtd2 D-aminoacyl-tRNA deacylase 2 JBrowse link 6 72,781,229 72,786,835 RGD:8554872
G Gpr33 G protein-coupled receptor 33 JBrowse link 6 72,804,843 72,805,848 RGD:8554872
G Heatr5a HEAT repeat containing 5A JBrowse link 6 72,648,654 72,750,202 RGD:8554872
G Nubpl nucleotide binding protein-like JBrowse link 6 72,891,758 73,147,837 RGD:8554872
RGD:7240710

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15608
    Nutritional and Metabolic Diseases 4389
      disease of metabolism 4389
        mitochondrial metabolism disease 314
          mitochondrial complex I deficiency 60
            Mitochondrial Complex I Deficiency, Nuclear Type 21 4
Path 2
Term Annotations click to browse term
  disease 15608
    Developmental Diseases 8985
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7801
        genetic disease 7294
          inherited metabolic disorder 1908
            mitochondrial metabolism disease 314
              mitochondrial complex I deficiency 60
                Mitochondrial Complex I Deficiency, Nuclear Type 21 4
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.