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Human Disease and Mouse Model Detail
Human Disease Congenital Disorder of Glycosylation, Type IB; CDG1B
OMIM ID: 602579
Synonyms Cdg IB; CDGIB; CDG, Gastrointestinal Type; Congenital Disorders of Glycosylation, Type I; Mannosephosphate Isomerase Deficiency; MPI Deficiency; Protein-Losing Enteropathy-Hepatic Fibrosis Syndrome; Saguenay-Lac Saint-Jean Syndrome; SLSJ SYNDROME
View all models View ALL (1) "NOT" mouse models for this human disease. No mouse models with similarity to the expected human disease phenotype are reported in MGI.
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Gene is associated with the disease in this species
      Mouse Homologs Human Homologs Mouse Models Mouse : Human
Homology Class
     Mpi MPI* View 1 "NOT" model 1:1 Homology

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
07/15/2014
MGI 5.18
The Jackson Laboratory