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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 15603
    Nutritional and Metabolic Diseases 4390
      disease of metabolism 4390
        mitochondrial metabolism disease 308
          mitochondrial complex I deficiency 57
            Mitochondrial Complex I Deficiency, Nuclear Type 21 4
Path 2
Term Annotations click to browse term
  disease 15603
    Developmental Diseases 8772
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7555
        genetic disease 7051
          inherited metabolic disorder 1877
            mitochondrial metabolism disease 308
              mitochondrial complex I deficiency 57
                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.