Symbol Name ID |
Fgfr2
fibroblast growth factor receptor 2 MGI:95523 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Increased level of L-fucose in urine |
Hypospadias |
Coronal hypospadias |
Abnormal renal morphology |
Hydronephrosis |
Nephrosclerosis |
Renal agenesis |
Disease(s) Associated with FGFR2 | |||||||
acrocephalosyndactylia | |||||||
Antley-Bixler syndrome without disordered steroidogenesis | |||||||
Beare-Stevenson cutis gyrata syndrome | |||||||
lacrimoauriculodentodigital syndrome 1 | |||||||
stomach cancer |
Mouse Phenotypes | renal/urinary system phenotype |
abnormal kidney cortex morphology |
decreased renal glomerulus number |
abnormal kidney development |
small kidney |
decreased nephron number |
dilated distal convoluted tubule |
dilated proximal convoluted tubule |
abnormal urethra morphology |
hypospadia |
perineal hypospadia |
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Availability | Mouse Genotype | |||||||||||
Fgfr2m1Sgg/Fgfr2m1Sgg | ||||||||||||
Fgfr2tm1.1Dsn/Fgfr2tm1.1Dsn | ||||||||||||
Fgfr2tm3.1Lni/Fgfr2tm3.1Lni | * | |||||||||||
Fgfr2tm3Dsn/Fgfr2tm3Dsn | ||||||||||||
Fgfr2tm3Lni/Fgfr2tm3Lni | ||||||||||||
Fgfr2tm2.3Dsn/Fgfr2+ |
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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