Symbol Name ID |
Mmp9
matrix metallopeptidase 9 MGI:97011 |
Darker colors indicate more annotations |
Human Phenotypes | Retinal arteritis |
Keratoconjunctivitis sicca |
Blepharitis |
Keratoconus |
Cataract |
Abnormality iris morphology |
Abnormal iris pigmentation |
Brushfield spots |
Iris flocculi |
Optic atrophy |
Hypertelorism |
Strabismus |
Nystagmus |
Ophthalmoparesis |
Myopia |
Diplopia |
Amaurosis fugax |
Visual impairment |
Amblyopia |
Blindness |
Visual field defect |
Visual loss |
Ptosis |
Disease(s) Associated with MMP9 | |||||||||||||||||||||||
Down syndrome | |||||||||||||||||||||||
Sjogren's syndrome | |||||||||||||||||||||||
temporal arteritis | |||||||||||||||||||||||
thoracic aortic aneurysm |
Mouse Phenotypes | abnormal induced retina neovascularization |
abnormal retina apoptosis |
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Availability | Mouse Genotype | ||
Mmp9tm1Tvu/Mmp9tm1Tvu |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 04/16/2024 MGI 6.23 |
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