Human Disease and Mouse Model Detail
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Human Disease
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Megaloblastic Anemia 1
OMIM ID: 261100
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Synonyms
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Enterocyte Cobalamin Malabsorption;
Enterocyte Intrinsic Factor Receptor, Defect of;
Imerslund-Grasbeck Syndrome; IGS;
Mga1;
Pernicious Anemia, Juvenile, Due to Selective Intestinal Malabsorption of Vitamin B12, with Proteinuria
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Genes and
mouse models
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Mutations in human and/or mouse homologs are associated with this disease
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*Gene is associated with the disease in this species |
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Amn
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AMN*
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1:1 Homology
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Cubn
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CUBN*
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1:1 Homology
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Analysis Tools