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Symbol
Name
ID
Fgfr2
fibroblast growth factor receptor 2
MGI:95523
Phenotype annotations related to muscle
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
Availability Mouse Genotype
Fgfr2tm1.1Dsn/Fgfr2tm1.1Dsn
Fgfr2tm3Dsn/Fgfr2tm3Dsn
Fgfr2tm1Ewj/Fgfr2+
Tg(EIIa-cre)C5379Lmgd/0  (conditional)

Contributing Projects:
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
The Jackson Laboratory