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Symbol Name ID |
Fgfr1
fibroblast growth factor receptor 1 MGI:95522 |
| Darker colors indicate more annotations |
| Human Phenotypes | Camptodactyly of finger |
| Disease(s) Associated with FGFR1 | |
| osteoglophonic dysplasia |
| Mouse Phenotypes | abnormal myocardial fiber morphology |
thin myocardium |
abnormal fetal cardiomyocyte proliferation |
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| Availability | Mouse Genotype | |||
| Fgfr1tm1Upir/Fgfr1tm1.1Upir (conditional) | ||||
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 04/09/2024 MGI 6.23 |
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