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Human Disease and Mouse Model Detail
Human Disease Osteogenesis Imperfecta, Type II; OI2
OMIM ID: 166210
Human Phenotype Ontology associations
Synonyms OI, Type II; Osteogenesis Imperfecta; Osteogenesis Imperfecta Congenita, Perinatal Lethal Form; Osteogenesis Imperfecta Congenita; OIC; Vrolik Type of Osteogenesis Imperfecta
View all models View ALL (3) 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
     COL1A1* Col1a1* View 2 models HomoloGene and HGNC
     SMPD3 Smpd3* View 1 model HomoloGene and HGNC
     COL1A2* Col1a2   HomoloGene and HGNC
References Disease References using Mouse Models (3)

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