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Human Disease and Mouse Model Detail
Human Disease Congenital Disorder of Glycosylation, Type Im; CDG1M
OMIM ID: 610768
Synonyms Cdg Im; CDGIM; Congenital Disorders of Glycosylation, Type I; Dk1 Deficiency; Dolichol Kinase Deficiency
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
     Dolk DOLK*   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
09/09/2014
MGI 5.19
The Jackson Laboratory