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Details
Link-It Detail - Jax Mouse Phenotype - hemochromatosis
Debug Stats
  • ### Total Build Time: 25 ms 7.999 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 358 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 308 bytes
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  • CONCEPT_SEMANTIC_TYPE gt=9 ms Completed: 9 ms rowSize= 14 bytes
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  • CONCEPT_PARENTS gt=3 ms Completed: 3 ms rowSize= 574 bytes
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  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.573 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=11 ms Completed: 11 ms rowSize= 3.909 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.153 KB
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Jax Mouse Phenotype (1)
hemochromatosis MP:0005638
Definition (1)
disorder due to the deposition of hemosiderin in the parenchymal cells, causing tissue damage and dysfunction of the liver, pancreas, heart, and pituitary
Parents (1)
img abnormal iron level MP:0001770
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img homeostasis/metabolism phenotype MP:00053767img abnormal iron level MP:0001770
Genes (6)

Species:
human : 6
SpeciesGeneGeneIdGene NameEvidence
HumanHFE2148738hemochromatosis type 2 (juvenile)
Click here to display 18 evidence detail records.
HumanTFR27036transferrin receptor 2
Click here to display 18 evidence detail records.
HumanTF7018transferrin
Click here to display 18 evidence detail records.
HumanHFE3077hemochromatosis
Click here to display 18 evidence detail records.
HumanCP1356ceruloplasmin (ferroxidase)
Click here to display 18 evidence detail records.
HumanB2M567beta-2-microglobulin
Click here to display 18 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0005638hemochromatosis0self