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Human Disease and Mouse Model Detail
Human Disease Osteogenesis Imperfecta, Type IV
OMIM ID: 166220
Synonyms Oi4; OI, Type IV; Osteogenesis Imperfecta; Osteogenesis Imperfecta with Normal Sclerae
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
     Col1a1 COL1A1*   1:1 Homology
Col1a2 COL1A2*   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
11/18/2014
MGI 5.20
The Jackson Laboratory