|
Symbol Name ID |
Fgfr1
fibroblast growth factor receptor 1 MGI:95522 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Shallow orbits |
Iris coloboma |
Hypertelorism |
Proptosis |
Strabismus |
Myopia |
Ptosis |
| Disease(s) Associated with FGFR1 | |||||||
| acrocephalosyndactylia | |||||||
| hypogonadotropic hypogonadism 2 with or without anosmia | |||||||
| Jackson-Weiss syndrome | |||||||
| osteoglophonic dysplasia | |||||||
| Pfeiffer syndrome |
| Mouse Phenotypes | vision/eye phenotype |
ocular hypertelorism |
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| Availability | Mouse Genotype | ||
| Fgfr1tm2.1Cxd/Fgfr1tm2.1Cxd | |||
| Fgfr1Eask/Fgfr1+ | * | ||
| Fgfr1tm2.1Cxd/Fgfr1+ | |||
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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