Symbol Name ID |
Fgfr3
fibroblast growth factor receptor 3 MGI:95524 |
Darker colors indicate more annotations |
Human Phenotypes | Decreased fetal movement |
Feeding difficulties |
Feeding difficulties in infancy |
Bowel incontinence |
Urinary incontinence |
Autism |
Attention deficit hyperactivity disorder |
Disease(s) Associated with FGFR3 | |||||||
achondroplasia | |||||||
craniosynostosis | |||||||
Muenke Syndrome | |||||||
SADDAN | |||||||
thanatophoric dysplasia |
Mouse Phenotypes | abnormal behavior |
absent gastric milk in neonates |
abnormal gait |
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Availability | Mouse Genotype | |||
Fgfr3tm1Dor/Fgfr3tm1Dor | ||||
Fgfr3tm1Led/Fgfr3tm1Led | ||||
Fgfr3tm3Cxd/Fgfr3tm3Cxd | ||||
Fgfr3tm5Cxd/Fgfr3tm5Cxd |
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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