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Human Disease and Mouse Model Detail
Human Disease Congenital Disorder of Glycosylation, Type Iim; CDG2M
OMIM ID: 300896
Human Phenotype Ontology associations
Synonyms Cdg Iim; CDGIIM; Congenital Disorders of Glycosylation, Type II; Epileptic Encephalopathy, Early Infantile, 22; EIEE22; Mental Retardation, Autosomal Dominant
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
     SLC35A2* Slc35a2   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