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MAMMALIAN PHENOTYPE - ANNOTATIONS

The Mouse Adult Gross Anatomy Ontology and Mammalian Phenotype Ontology are downloaded weekly from the Mouse Genome Informatics databases at Jackson Laboratories (ftp://ftp.informatics.jax.org/pub/reports/index.html). For more information about these ontologies, see the MGI Publications Page at http://www.informatics.jax.org/mgihome/other/publications.shtml.

Term:abnormal circulating iron level
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Accession:MP:0004152 term browser browse the term
Definition:anomalous blood concentration of the metallic element that normally occurs in the heme of hemoglobin, myoglobin, transferrin, ferritin, and iron-containing porphyrins; it is an essential component of enzymes such as catalase, peroxidase, and various cytochromes
Comment:Serum iron measures the total amount of iron in the blood, nearly all of which is bound to transferrin.



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decreased circulating iron level term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Cp ceruloplasmin IMP RGD PMID:31560858 RGD:38549582 NCBI chr 2:102,439,433...102,498,075
Ensembl chr 2:102,439,624...102,498,075
JBrowse link
G Cpem1Ang ceruloplasmin; CRISPR/Cas9 induced mutant1, Ang IMP RGD PMID:31560858 RGD:38549582

Term paths to the root
Path 1
Term Annotations click to browse term
  mammalian phenotype 5374
    homeostasis/metabolism phenotype 1396
      abnormal homeostasis 1299
        abnormal blood homeostasis 743
          abnormal circulating mineral level 37
            abnormal circulating iron level 3
              decreased circulating iron level 3
              increased circulating iron level 0
Path 2
Term Annotations click to browse term
  mammalian phenotype 5374
    homeostasis/metabolism phenotype 1396
      abnormal homeostasis 1299
        abnormal mineral homeostasis 53
          abnormal mineral level 52
            abnormal iron level 7
              abnormal circulating iron level 3
                decreased circulating iron level 3
                increased circulating iron level 0
paths to the root