Symbol Name ID |
Col1a1
collagen, type I, alpha 1 MGI:88467 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Abnormality of iron homeostasis |
Nonimmune hydrops fetalis |
Abnormality of temperature regulation |
Fever |
Hypercalciuria |
Atrophic scars |
Exercise intolerance |
Disease(s) Associated with COL1A1 | |||||||
beta thalassemia | |||||||
Caffey disease | |||||||
Ehlers-Danlos syndrome arthrochalasia type 1 | |||||||
osteogenesis imperfecta | |||||||
osteogenesis imperfecta type 2 |
Mouse Phenotypes | homeostasis/metabolism phenotype |
decreased hydroxyproline level |
abnormal blood gas level |
increased circulating parathyroid hormone level |
decreased circulating alkaline phosphatase level |
abnormal enzyme/coenzyme level |
abnormal hormone level |
decreased collagen level |
abnormal bone healing |
decreased susceptibility to injury |
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Availability | Mouse Genotype | ||||||||||
Col1a1m1Btlr/Col1a1m1Btlr | |||||||||||
Col1a1tm1Dab/Col1a1tm1Dab | |||||||||||
Col1a1Aga2/Col1a1+ | |||||||||||
Col1a1M1Jrt/Col1a1+ | * |
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 08/02/2024 MGI 6.24 |
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