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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 intestine copper level
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Accession:MP:0010246 term browser browse the term
Definition:an anomaly in the amount of copper present in the intestine


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decreased intestine copper level term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Slc39a4 solute carrier family 39 (zinc transporter), member 4 IAGP MGI PMID:22737083 NCBI chr15:76,496,583...76,501,579
Ensembl chr15:76,496,583...76,501,584 		JBrowse link
increased intestine copper level term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Atp7a ATPase, copper transporting, alpha polypeptide IAGP MGI PMID:4858102 PMID:6685755 PMID:7333461 PMID:8640230 NCBI chr  X:105,070,830...105,171,766
Ensembl chr  X:105,070,882...105,168,532 		JBrowse link
Term paths to the root
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  mammalian phenotype 16962
    homeostasis/metabolism phenotype 7866
      abnormal homeostasis 7015
        abnormal mineral homeostasis 1108
          abnormal mineral level 1098
            abnormal copper level 17
              abnormal intestine copper level 2
                decreased intestine copper level 1
                increased intestine copper level 1
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