Symbol Name ID |
Fgfr3
fibroblast growth factor receptor 3 MGI:95524 |
Darker colors indicate more annotations |
Human Phenotypes | Conjunctivitis |
Hepatosplenomegaly |
Recurrent otitis media |
Inflammatory abnormality of the eye |
Brain abscess |
Disease(s) Associated with FGFR3 | |||||
achondroplasia | |||||
Crouzon syndrome-acanthosis nigricans syndrome | |||||
lacrimoauriculodentodigital syndrome 2 | |||||
Muenke Syndrome | |||||
SADDAN | |||||
thanatophoric dysplasia |
Mouse Phenotypes | abnormal osteoclast differentiation |
increased osteoclast cell number |
abnormal osteoclast physiology |
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Availability | Mouse Genotype | |||
Fgfr3tm1Led/Fgfr3tm1Led | ||||
Fgfr3tm3.1Cxd/Fgfr3tm3.1Cxd | ||||
Tg(Col2a1-Fgfr3/GH)BDor/0 | ||||
Fgfr3tm2Llm/Fgfr3+ Tg(CMV-cre)1Ipc/? (conditional) |
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Fgfr3tm2Llm/Fgfr3+ Tg(Col2a1-cre)1Bhr/? (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 04/23/2024 MGI 6.23 |
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