About   Help   FAQ
Human Disease and Mouse Model Detail
Human Disease Microphthalmia, Syndromic 9; MCOPS9
OMIM ID: 601186
Synonyms Anophthalmia, Clinical, with Mild Facial Dysmorphism and Variable Malformations of the Lung, Heart, and Diaphragm; Anophthalmia/Microphthalmia and Pulmonary Hypoplasia; Matthew-Wood Syndrome; Microphthalmia, Isolated, with Coloboma; Microphthalmia, Syndromic; Spear Syndrome
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
     STRA6* Stra6   HomoloGene and HGNC

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
08/18/2015
MGI 6.0
The Jackson Laboratory