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Human Disease and Mouse Model Detail
Human Disease Congenital Disorder of Glycosylation, Type IIA; CDG2A
OMIM ID: 212066
Human Phenotype Ontology associations
Synonyms Alkuraya Syndrome; Carbohydrate-Deficient Glycoprotein Syndrome, Type II, Formerly; CDGS2, FORMERLY; Cdg IIA; CDGIIA; Congenital Disorders of Glycosylation, Type II; Mental Retardation, Growth Retardation, Prominent Columella, and Open Mouth
View all models View ALL (2) mouse models for this human disease.
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
     MGAT2* Mgat2* View 2 models HomoloGene and HGNC
References Disease References using Mouse Models (1)

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