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Symbol
Name
ID
Mmp9
matrix metallopeptidase 9
MGI:97011
Phenotype annotations related to cardiovascular system
Darker colors indicate more annotations
Human Phenotypes
Subarachnoid hemorrhage
Bruising susceptibility
Retinal arteritis
Keratoconjunctivitis sicca
Abnormal cardiovascular system morphology
Atrial septal defect
Patent foramen ovale
Secundum atrial septal defect
Ventricular septal defect
Perimembranous ventricular septal defect
Atrioventricular canal defect
Complete atrioventricular canal defect
Double outlet right ventricle
Double outlet right ventricle with subpulmonary ventricular septal defect without pulmonary stenosis
Tetralogy of Fallot
Bicuspid aortic valve
Ebstein anomaly of the tricuspid valve
Pericarditis
Cardiomegaly
Ascending aortic dissection
Aortic aneurysm
Abdominal aortic aneurysm
Thoracic aortic aneurysm
Aortic root aneurysm
Ascending tubular aorta aneurysm
Descending thoracic aorta aneurysm
Aortic dissection
Descending aortic dissection
Aortic rupture
Mucoid extracellular matrix accumulation
Pulmonary artery stenosis
Partial anomalous pulmonary venous return
Patent ductus arteriosus
Carotid artery dilatation
Carotid artery stenosis
Anterior cerebral artery stenosis
Middle cerebral artery stenosis
Posterior cerebral artery stenosis
Dilatation of the cerebral artery
Moyamoya phenomenon
Coronary artery aneurysm
Coronary artery atherosclerosis
Premature coronary artery atherosclerosis
Coronary artery dissection
Peripheral arterial stenosis
Cystic medial necrosis
Varicose veins
Vasculitis
Stroke
Ischemic stroke
Transient ischemic attack
Abnormal left ventricular function
Aortic regurgitation
Pulmonic stenosis
Hypertension
Cerebral ischemia
Hypovolemia
Arrhythmia
Sudden cardiac death
Myocardial infarction
Abnormality of the lymphatic system
Mediastinal lymphadenopathy
Cutis marmorata
Livedo reticularis
Telangiectasia
Disease(s) Associated with MMP9
coronary artery disease
Down syndrome
Sjogren's syndrome
systemic scleroderma
temporal arteritis
thoracic aortic aneurysm
varicose veins
ventricular septal defect

Mouse Phenotypes
abnormal induced retina neovascularization
abnormal angiogenesis
abnormal physiological neovascularization
increased angiogenesis
thick interventricular septum
increased heart left ventricle posterior wall thickness
cardiac fibrosis
increased susceptibility to dystrophic cardiac calcinosis
decreased susceptibility to induced aneurysm formation
decreased cardiac muscle contractility
increased ventricle muscle contractility
abnormal impulse conducting system conduction
abnormal myocardial fiber physiology
abnormal response to cardiac infarction
decreased myocardial infarct size
enhanced blood-brain barrier function
increased vascular permeability
abnormal vascular smooth muscle physiology
abnormal vascular wound healing
myocarditis
Availability Mouse Genotype
Mmp9tm1Amr/Mmp9tm1Amr
Mmp9tm1Arnd/Mmp9tm1Arnd
Mmp9tm1Tvu/Mmp9tm1Tvu
Mmp9tm1Amr/Mmp9+

Contributing Projects:
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
The Jackson Laboratory