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Symbol
Name
ID

Abcg2
ATP binding cassette subfamily G member 2 (Junior blood group)
MGI:1347061

Phenotype annotations related to digestive/alimentary system

Darker colors indicate more annotations

Human Phenotypes	Functional abnormality of the gastrointestinal tract
Disease(s) Associated with ABCG2	Functional abnormality of the gastrointestinal tract
multiple myeloma

Mouse Phenotypes		abnormal intestine physiology
Availability	Mouse Genotype	abnormal intestine physiology
	Abcg2^em1Omw/Abcg2^em1Omw

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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