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Human Disease and Mouse Model Detail
Human Disease Congenital Disorder of Glycosylation, Type Ic; CDG1C
OMIM ID: 603147
Human Phenotype Ontology associations
Synonyms Carbohydrate-Deficient Glycoprotein Syndrome, Type I, with Deficient Glycosylation of Dolichol-Linked Oligosaccharide, Formerly; Carbohydrate-Deficient Glycoprotein Syndrome, Type V, Formerly; CDGS5, FORMERLY; Cdg Ic; CDGIC; Congenital Disorders of Glycosylation, Type I
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
     ALG6* Alg6   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