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Human Disease and Mouse Model Detail
Human Disease Megaloblastic Anemia 1
OMIM ID: 261100
Human Phenotype Ontology associations
Synonyms Enterocyte Cobalamin Malabsorption; Enterocyte Intrinsic Factor Receptor, Defect of; Imerslund-Grasbeck Syndrome; IGS; Megaloblastic Anemia; Mga1; Pernicious Anemia, Juvenile, Due to Selective Intestinal Malabsorption of Vitamin B12, with Proteinuria
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Disease is associated/modeled with this Gene or a homolog. More...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     AMN* Amn   HomoloGene and HGNC
CUBN* Cubn   HomoloGene and HGNC

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
MGI 6.07
The Jackson Laboratory