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Symbol Name ID |
Crtap
cartilage associated protein MGI:1891221 |
| Darker colors indicate more annotations |
| Human Phenotypes | Decreased calvarial ossification |
Delayed cranial suture closure |
Wide cranial sutures |
Wormian bones |
Wide anterior fontanel |
Dentinogenesis imperfecta |
Bowing of the legs |
Coxa vara |
Femoral retroversion |
Protrusio acetabuli |
Micromelia |
Rhizomelia |
Multiple prenatal fractures |
Recurrent fractures |
Crumpled long bones |
Multiple rib fractures |
Pectus excavatum |
Narrow chest |
Scoliosis |
Vertebral compression fracture |
Osteopenia |
| Disease(s) Associated with CRTAP | |||||||||||||||||||||
| osteogenesis imperfecta type 7 |
| Mouse Phenotypes | abnormal osteoblast physiology |
disorganized long bone epiphyseal plate |
decreased length of long bones |
kyphoscoliosis |
abnormal bone structure |
abnormal trabecular bone morphology |
decreased bone mass |
osteoporosis |
abnormal bone mineralization |
decreased bone ossification |
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| Availability | Mouse Genotype | ||||||||||
| Crtaptm1Brle/Crtaptm1Brle | |||||||||||
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 05/14/2024 MGI 6.23 |
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