Symbol Name ID |
Fgfr2
fibroblast growth factor receptor 2 MGI:95523 |
Darker colors indicate more annotations |
Human Phenotypes | Hypoplastic labia majora |
Fused labia minora |
Hypospadias |
Coronal hypospadias |
Bifid scrotum |
Prominent scrotal raphe |
Cryptorchidism |
Vaginal atresia |
Dysgerminoma |
Disease(s) Associated with FGFR2 | |||||||||
acrocephalosyndactylia | |||||||||
Antley-Bixler syndrome without disordered steroidogenesis | |||||||||
Beare-Stevenson cutis gyrata syndrome | |||||||||
craniosynostosis | |||||||||
Crouzon syndrome | |||||||||
lacrimoauriculodentodigital syndrome 1 | |||||||||
Saethre-Chotzen syndrome |
Mouse Phenotypes | abnormal perineum morphology |
abnormal decidualization |
abnormal prostate gland branching morphogenesis |
decreased prostate gland duct number |
increased prostate gland weight |
abnormal seminal vesicle morphology |
abnormal seminal vesicle development |
abnormal branching involved in seminal vesicle morphogenesis |
abnormal seminal vesicle muscle layer morphology |
primary sex reversal |
female infertility |
reduced male fertility |
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Availability | Mouse Genotype | ||||||||||||
Fgfr2hob/Fgfr2hob | |||||||||||||
Fgfr2svs/Fgfr2svs | |||||||||||||
Fgfr2tm1.1Dsn/Fgfr2tm1.1Dsn | |||||||||||||
Fgfr2tm1Lni/Fgfr2tm1Lni | |||||||||||||
Fgfr2tm1.1Dor/Fgfr2hob | |||||||||||||
Fgfr2tm1.1Dor/Fgfr2svs | |||||||||||||
Fgfr2tm2Cxd/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 04/30/2024 MGI 6.23 |
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