About   Help   FAQ
Human Disease and Mouse Model Detail
Human Disease Microphthalmia, Syndromic 13; MCOPS13
OMIM ID: 300915
Synonyms Colobomatous Microphthalmia with Microcephaly, Short Stature, and Psychomotor Retardation; Maine Microphthalmos; Microphthalmia, Syndromic
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
     HMGB3*   0:1 Homology

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
08/26/2014
MGI 5.19
The Jackson Laboratory