Symbol Name ID |
Mmp9
matrix metallopeptidase 9 MGI:97011 |
Darker colors indicate more annotations |
Human Phenotypes | Brachycephaly |
Retrognathia |
Malar flattening |
Abnormality of the fontanelles or cranial sutures |
Short neck |
Short middle phalanx of the 5th finger |
Clinodactyly of the 5th finger |
Arachnodactyly |
Sandal gap |
Clinodactyly |
Brachydactyly |
Short palm |
Shallow acetabular fossae |
Abnormal fetal nasal bone visualization |
Joint hypermobility |
Joint stiffness |
Delayed skeletal maturation |
Hypoplastic iliac wing |
Abnormal sternum morphology |
Scoliosis |
Atlantoaxial dislocation |
Atlantoaxial instability |
Osteoporosis |
Arthritis |
Gout |
Rheumatoid arthritis |
Disease(s) Associated with MMP9 | ||||||||||||||||||||||||||
coronary artery disease | ||||||||||||||||||||||||||
Down syndrome | ||||||||||||||||||||||||||
Sjogren's syndrome | ||||||||||||||||||||||||||
temporal arteritis | ||||||||||||||||||||||||||
thoracic aortic aneurysm |
Mouse Phenotypes | joint swelling |
decreased susceptibility to induced arthritis |
joint inflammation |
short femur |
short tibia |
abnormal metatarsal bone morphology |
abnormal long bone epiphyseal plate morphology |
abnormal long bone hypertrophic chondrocyte zone |
increased width of hypertrophic chondrocyte zone |
decreased length of long bones |
abnormal trabecular bone morphology |
osteopetrosis |
delayed bone ossification |
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Availability | Mouse Genotype | |||||||||||||
Mmp9tm1b(EUCOMM)Wtsi/Mmp9tm1b(EUCOMM)Wtsi | ||||||||||||||
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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