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Symbol Name ID |
Phex
phosphate regulating endopeptidase homolog, X-linked MGI:107489 |
| Darker colors indicate more annotations |
| Human Phenotypes | Frontal bossing |
Enamel hypomineralization |
| Disease(s) Associated with PHEX | ||
| X-linked dominant hypophosphatemic rickets |
| Mouse Phenotypes | abnormal craniofacial bone morphology |
abnormal cranial suture morphology |
abnormal cranium morphology |
decreased cranium height |
small cranium |
short frontal bone |
abnormal temporal bone morphology |
short mandible |
short premaxilla |
short maxilla |
short nasal bone |
domed cranium |
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| Availability | Mouse Genotype | ||||||||||||
| PhexHyp/PhexHyp | |||||||||||||
| PhexHyp-2J/Y | |||||||||||||
| PhexHyp-Duk/Y | |||||||||||||
| PhexHyp/Y | |||||||||||||
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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