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Human Disease and Mouse Model Detail
Human Disease Microphthalmia, Syndromic 7; MCOPS7
OMIM ID: 309801
Synonyms Microphthalmia with Linear Skin Defects; MLS; Microphthalmia, Dermal Aplasia, and Sclerocornea; Microphthalmia, Syndromic; Midas Syndrome
View all models View ALL (9) mouse models for this human disease.
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
     Hccs* HCCS* View 3 models 1:1 Homology
     Arhgap6* ARHGAP6 View 3 models 1:1 Homology
Mid1* MID1 View 3 models 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
10/08/2014
MGI 5.20
The Jackson Laboratory