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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:Fanconi anemia complementation group J
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Accession:DOID:0111097 term browser browse the term
Definition:A Fanconi anemia that has_material_basis_in homozygous or compound heterozygous mutation in the BRIP1 gene on chromosome 17q22. (DO)
Synonyms:exact_synonym: FANCJ
 narrow_synonym: BRIP1-RELATED DISORDER
 primary_id: MESH:C563801
 alt_id: OMIM:609054;   RDO:0012967
For additional species annotation, visit the Alliance of Genome Resources.

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Fanconi anemia complementation group J term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Brip1 BRCA1 interacting protein C-terminal helicase 1 ISO ClinVar Annotator: match by OMIM:609054
DNA:nonsense mutation:cds:p.R798* (human)
ClinVar Annotator: match by term: Fanconi anemia, complementation group J
PMID:11301010, PMID:12565990, PMID:12569564, PMID:12872252, PMID:14983014, PMID:15285897, PMID:16116421, PMID:16116423, PMID:16116424, PMID:16153896, PMID:16280053, PMID:16430786, PMID:16973432, PMID:17033622, PMID:17145708, PMID:17342202, PMID:17596542, PMID:18414782, PMID:18426915, PMID:18483852, PMID:18510924, PMID:18628483, PMID:19099189, PMID:19127258, PMID:19150983, PMID:19197335, PMID:19339519, PMID:19379763, PMID:19442249, PMID:19519404, PMID:19584272, PMID:19763819, PMID:19935797, PMID:20068231, PMID:20159562, PMID:20168331, PMID:20177395, PMID:20639400, PMID:20980836, PMID:21127055, PMID:21165771, PMID:21279724, PMID:21345144, PMID:21356067, PMID:21409391, PMID:21964575, PMID:22006311, PMID:22024395, PMID:22287629, PMID:22582397, PMID:22692731, PMID:22792074, PMID:23161009, PMID:23276657, PMID:23555315, PMID:23613520, PMID:23644138, PMID:23935105, PMID:24033266, PMID:24123366, PMID:24240112, PMID:24376576, PMID:24448499, PMID:24487782, PMID:24556621, PMID:24573678, PMID:24584348, PMID:24728327, PMID:24755471, PMID:24763289, PMID:24895130, PMID:25058500, PMID:25186627, PMID:25256751, PMID:25318351, PMID:25374583, PMID:25452441, PMID:25525159, PMID:25583461, PMID:25722345, PMID:25741868, PMID:25846551, PMID:25980754, PMID:25981591, PMID:26206375, PMID:26207792, PMID:26264438, PMID:26296696, PMID:26315354, PMID:26467025, PMID:26483394, PMID:26534844, PMID:26556299, PMID:26580448, PMID:26596371, PMID:26635394, PMID:26659599, PMID:26681312, PMID:26681682, PMID:26689913, PMID:26709662, PMID:26720728, PMID:26757417, PMID:26786923, PMID:26790966, PMID:26822149, PMID:26822949, PMID:26824983, PMID:26845104, PMID:26901136, PMID:26911350, PMID:26921362, PMID:26968956, PMID:26976419, PMID:27074266, PMID:27107905, PMID:27150160, PMID:27153395, PMID:27165003, PMID:27179029, PMID:27193682, PMID:27378695, PMID:27427815, PMID:27433846, PMID:27443514, PMID:27498913, PMID:27527004, PMID:27547810, PMID:27553368, PMID:27621404, PMID:27701467, PMID:27978560, PMID:27997549, PMID:28076423, PMID:28135145, PMID:28152038, PMID:28202063, PMID:28423363, PMID:28492532, PMID:28495237, PMID:28503720, PMID:28528518, PMID:28678401, PMID:28709830, PMID:28717660, PMID:28767289, PMID:28796317, PMID:28911102, PMID:28961279, PMID:29263802, PMID:29335925, PMID:29338689, PMID:29360161, PMID:29368626, PMID:29470806, PMID:29625052, PMID:29636988, PMID:29667044, PMID:29788478, PMID:29922827, PMID:29929473, PMID:30086788, PMID:30093976, PMID:30130155, PMID:30230034, PMID:30262796, PMID:30295334, PMID:30311386, PMID:30322717, PMID:30374176, PMID:30414346, PMID:30728895, PMID:30982232, PMID:31159747, PMID:31214711, PMID:31265121, PMID:31341520, PMID:31822495, PMID:31843900, PMID:32566746, PMID:26968956 RGD:11251781 NCBI chr10:73,507,009...73,632,742
Ensembl chr10:73,507,100...73,629,581
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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16103
    Developmental Diseases 9506
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8364
        genetic disease 7847
          monogenic disease 5622
            Fanconi anemia complementation group J 1
Path 2
Term Annotations click to browse term
  disease 16103
    disease of anatomical entity 15351
      Hemic and Lymphatic Diseases 2045
        hematopoietic system disease 1641
          bone marrow disease 473
            Bone Marrow Failure Disorders 162
              aplastic anemia 150
                congenital hypoplastic anemia 107
                  Fanconi anemia 43
                    Fanconi anemia complementation group J 1
paths to the root


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.