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Symbol Name ID |
Fgf8
fibroblast growth factor 8 MGI:99604 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Delayed skeletal maturation |
| Disease(s) Associated with FGF8 | |
| hypogonadotropic hypogonadism 6 with or without anosmia |
| Mouse Phenotypes | skeleton phenotype |
absent Meckel's cartilage |
absent molars |
abnormal mandible morphology |
abnormal maxilla morphology |
absent incus |
abnormal calcaneum morphology |
absent deltoid tuberosity |
absent radius |
abnormal limb bone morphology |
abnormal skeleton development |
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| Availability | Mouse Genotype | |||||||||||
| Fgf8tm1.2Mrt/Fgf8tm1.3Mrt Tg(Nes-cre)1Atp/0 (conditional) |
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| Fgf8tm1.3Mrt/Fgf8tm1.4Mrt Tg(Msx2-cre)5Rem/0 (conditional) |
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| Fgf8tm1.3Mrt/Fgf8tm1.4Mrt Tg(T-cre)1Lwd/0 (conditional) |
* | |||||||||||
| Fgf8tm1Mrc/Fgf8tm2Mrc Tg(Rarb-cre)1Mrc/0 (conditional) |
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| Gt(ROSA)26Sortm1(Fgf8)Lma/Gt(ROSA)26Sor+ Tg(Msx2-cre)5Rem/0 (conditional) |
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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 |
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