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ONTOLOGY REPORT - ANNOTATIONS


Term:Fanconi anemia complementation group I
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Accession:DOID:0111091 term browser browse the term
Definition:A Fanconi anemia that has_material_basis_in homozygous or compound heterozygous mutation in the FANCI gene on chromosome 15q26. (DO)
Synonyms:exact_synonym: FANCI
 primary_id: MESH:C563802
 alt_id: OMIM:609053;   RDO:0012968
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Fanconi anemia complementation group I term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Fanci FA complementation group I JBrowse link 1 141,116,565 141,172,997 RGD:7240710
RGD:8554872
RGD:11344924
G Polg DNA polymerase gamma, catalytic subunit JBrowse link 1 141,172,117 141,188,893 RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15599
    Nutritional and Metabolic Diseases 4365
      disease of metabolism 4365
        DNA Repair-Deficiency Disorders 202
          Fanconi anemia 43
            Fanconi anemia complementation group I 2
Path 2
Term Annotations click to browse term
  disease 15599
    disease of anatomical entity 14927
      Hemic and Lymphatic Diseases 1704
        hematopoietic system disease 1425
          bone marrow disease 401
            aplastic anemia 150
              congenital hypoplastic anemia 104
                Fanconi anemia 43
                  Fanconi anemia complementation group I 2
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.