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 |
Mouse Phenotypes | embryo phenotype |
abnormal placenta vasculature |
abnormal embryo development |
abnormal developmental patterning |
abnormal endoderm development |
short rostral-caudal axis |
embryonic growth retardation |
decreased embryo size |
absent primitive endoderm |
abnormal egg cylinder morphology |
abnormal apical ectodermal ridge morphology |
absent apical ectodermal ridge |
absent limb buds |
absent blastocoele |
inner cell mass degeneration |
increased trophoblast giant cell number |
enlarged allantois |
abnormal placenta morphology |
abnormal spongiotrophoblast layer morphology |
absent placental labyrinth |
abnormal trophoblast layer morphology |
abnormal umbilical cord morphology |
abnormal placenta development |
failure of chorioallantoic fusion |
abnormal decidualization |
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Availability | Mouse Genotype | |||||||||||||||||||||||||
Fgfr2m1Sgg/Fgfr2m1Sgg | ||||||||||||||||||||||||||
Fgfr2tm1.1Dor/Fgfr2tm1.1Dor | ||||||||||||||||||||||||||
Fgfr2tm1.1Wrst/Fgfr2tm1.1Wrst | ||||||||||||||||||||||||||
Fgfr2tm1Cxd/Fgfr2tm1Cxd | ||||||||||||||||||||||||||
Fgfr2tm1Lni/Fgfr2tm1Lni | * | |||||||||||||||||||||||||
Fgfr2tm3Dsn/Fgfr2tm3Dsn | ||||||||||||||||||||||||||
Fgfr2m1Sgg/Fgfr2+ | ||||||||||||||||||||||||||
Fgfr2tm3.1Cxd/Fgfr2+ | ||||||||||||||||||||||||||
Fgfr2tm3Ewj/Fgfr2+ | ||||||||||||||||||||||||||
Fgfr2tm1Dor/Fgfr2tm1Dor Tg(Sftpc-cre)1Blh/0 (conditional) |
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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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