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Human Disease and Mouse Model Detail
Human Disease Microphthalmia, Syndromic 9; MCOPS9
OMIM ID: 601186
Human Phenotype Ontology associations
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
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last database update
MGI 6.07
The Jackson Laboratory