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Symbol Name ID |
Fgfr1
fibroblast growth factor receptor 1 MGI:95522 |
| Darker colors indicate more annotations |
| Human Phenotypes | Esophageal atresia |
Pyloric stenosis |
Hepatocellular carcinoma |
| Disease(s) Associated with FGFR1 | |||
| acrocephalosyndactylia | |||
| hepatocellular carcinoma |
| Mouse Phenotypes | abnormal palatal mesenchymal cell proliferation |
abnormal secondary palate development |
failure of palatal shelf elevation |
palatal shelves fail to meet at midline |
persistence of medial edge epithelium during palatal shelf fusion |
decreased palatal shelf size |
cleft primary palate |
abnormal palatal rugae morphology |
cleft secondary palate |
cleft palate |
complete cleft palate |
abnormal tongue position |
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| Availability | Mouse Genotype | ||||||||||||
| Fgfr1tm2Jrt/Fgfr1tm2Jrt | |||||||||||||
| Fgfr1tm9.1Sor/Fgfr1tm9.1Sor | |||||||||||||
| Fgfr1tm1Jpa/Fgfr1tm1Jpa H2az2Tg(Wnt1-cre)11Rth/H2az2+ (conditional) |
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| Fgfr1tm1Jpa/Fgfr1tm1.1Jpa H2az2Tg(Wnt1-cre)11Rth/H2az2+ (conditional) |
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| Fgfr1tm5.1Sor/Fgfr1tm9.1Sor H2az2Tg(Wnt1-cre)11Rth/H2az2+ (conditional) |
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| Fgfr1tm5.1Sor/Fgfr1tm10.1Sor H2az2Tg(Wnt1-cre)11Rth/H2az2+ (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 04/23/2024 MGI 6.23 |
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