Human Disease and Mouse Model Detail

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Human Disease

Term: Osteogenesis Imperfecta, Type IV
OMIM ID: 166220

Synonyms

Oi4; OI, Type IV; Osteogenesis Imperfecta with Normal Sclerae

Associated Genes

Orthologous mouse and human markers where mutations in one or both species have been associated with phenotypes characteristic of this disease.

Mouse Gene

Human Gene

Characteristics of this human disease are associated with mutations in...

Col1a1	COL1A1
Col1a2	COL1A2

...the human gene.
MGI data currently do not associate this disease with mutations in the orthologous mouse gene.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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