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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 bilirubin level
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Accession:MP:0001569 term browser browse the term
Definition:any anomaly in the concentration in the blood of the bile pigment bilirubin, normally found in the liver and in red blood cells
Synonyms:alt_id: MP:0000200



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decreased circulating bilirubin level term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Lrrk2 leucine-rich repeat kinase 2 IMP RGD PMID:23799078 RGD:13462048 NCBI chr 7:122,826,712...122,987,711
Ensembl chr 7:122,826,696...122,987,703
JBrowse link
G Lrrk2em1Sage leucine-rich repeat kinase 2; zinc finger nuclease induced mutant 1, Sigma Advanced Genetic Engineering Labs IMP RGD PMID:23799078 RGD:13462048
increased circulating bilirubin level term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Abcc2 ATP binding cassette subfamily C member 2 IAGP RGD PMID:19525466 RGD:14985241 NCBI chr 1:242,664,657...242,723,239
Ensembl chr 1:242,664,657...242,723,238
JBrowse link
G Abcc2TR- ATP binding cassette subfamily C member 2;transport deficient mutant , IAGP RGD PMID:19525466 RGD:14985241
G Atp7b ATPase copper transporting beta IAGP compared to LEA/Hok RGD PMID:30733544 PMID:17303181 RGD:25823141, RGD:2292672 NCBI chr16:69,952,286...70,024,404
Ensembl chr16:69,951,778...70,023,636
JBrowse link
G Atp7bhts ATPase copper transporting beta; hepatitis IAGP compared to LEA/Hok RGD PMID:17303181 PMID:30733544 RGD:2292672, RGD:25823141
G Ugt1a1 UDP glucuronosyltransferase family 1 member A1 treatment IAGP compared to Gunn rats RGD PMID:16337205 PMID:20323028 PMID:15753292 PMID:1127102 RGD:13432067, RGD:1354701, RGD:1354702, RGD:1354700 NCBI chr 9:88,801,344...88,808,465
Ensembl chr 9:88,713,184...88,808,465
JBrowse link
G Ugt1a1j UDP glucuronosyltransferase family 1 member A1, jaundice mutant treatment IAGP compared to Gunn rats RGD PMID:16337205 PMID:1127102 PMID:20323028 PMID:15753292 RGD:13432067, RGD:1354700, RGD:1354701, RGD:1354702

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  mammalian phenotype 5364
    homeostasis/metabolism phenotype 1389
      abnormal homeostasis 1295
        abnormal blood homeostasis 742
          abnormal circulating bilirubin level 14
            decreased circulating bilirubin level 4
            increased circulating bilirubin level 10
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