About   Help   FAQ
Human Disease and Mouse Model Detail
Human Disease Microphthalmia, Syndromic 3; MCOPS3
OMIM ID: 206900
Synonyms Anophthalmia, Clinical, with Associated Anomalies; Anophthalmia-Esophageal-Genital Syndrome; Microphthalmia and Esophageal Atresia Syndrome; 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
     Six6 SIX6*   1:1 Homology
Sox2 SOX2*   1:1 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
09/23/2014
MGI 5.19
The Jackson Laboratory