Symbol Name ID |
Fgfr2
fibroblast growth factor receptor 2 MGI:95523 |
Darker colors indicate more annotations |
Human Phenotypes | Small thenar eminence |
Joint contracture of the hand |
Flexion contracture |
Camptodactyly |
Hypotonia |
Generalized hypotonia |
Abdominal wall muscle weakness |
Disease(s) Associated with FGFR2 | |||||||
Antley-Bixler syndrome without disordered steroidogenesis | |||||||
craniosynostosis | |||||||
lacrimoauriculodentodigital syndrome 1 |
Mouse Phenotypes | abnormal trabecula carnea morphology |
thin left ventricle myocardium compact layer |
abnormal vasodilation |
absent hypodermis muscle layer |
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Availability | Mouse Genotype | ||||
Fgfr2tm1.1Dsn/Fgfr2tm1.1Dsn | |||||
Fgfr2tm3Dsn/Fgfr2tm3Dsn | |||||
Fgfr2tm1Ewj/Fgfr2+ Tg(EIIa-cre)C5379Lmgd/0 (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 08/02/2024 MGI 6.24 |
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