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Human Disease and Mouse Model Detail
Human Disease

Term: Dubin-Johnson Syndrome; DJS
OMIM ID: 237500

Synonyms Hyperbilirubinemia, Dubin-Johnson Type; HBLRDJ; Hyperbilirubinemia II
Associated Genes

Orthologous mouse and human markers where mutations in one or both species have been associated with phenotypes characteristic of this disease.

Mouse Gene
Human Gene
 
Characteristics of this human disease are associated with mutations in...
     
Rdx RDX
  mouse...the mouse gene.
     OMIM data currently do not associate this disease with the orthologous human gene.
     
Abcc2 ABCC2
  human...the human gene.
     MGI data currently do not associate this disease with mutations in the orthologous mouse gene.
     

Mouse Models

Genotype Ref(s)
Allelic Composition Note Genetic Background
Models with phenotypic similarity to human disease where etiologies are distinct.1
Rdxtm1Sts/Rdxtm1Sts   involves: 129S4/SvJae * C57BL/6 J:77485

1Human genes are associated with this disease. Mouse model genotypes do not include mutations in the orthologs of these human genes.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
04/03/2013
MGI 5.12
The Jackson Laboratory