Symbol Name ID |
Phex
phosphate regulating endopeptidase homolog, X-linked MGI:107489 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Renal phosphate wasting |
Renal tubular dysfunction |
Disease(s) Associated with PHEX | ||
X-linked dominant hypophosphatemic rickets |
Mouse Phenotypes | renal/urinary system phenotype |
increased urine creatinine level |
abnormal renal glucose reabsorption |
abnormal renal phosphate reabsorption |
decreased urine calcium level |
abnormal urine nucleotide level |
increased urine phosphate level |
oliguria |
|
Availability | Mouse Genotype | ||||||||
PhexMhdabap024/Phex+ | * | ||||||||
PhexHyp/Y | |||||||||
PhexMhdabap024/Y | * | ||||||||
Phextm1.2Mkd/Y | |||||||||
Phextm1.1Mkd/Y Tg(BGLAP-cre)1Clem/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 04/23/2024 MGI 6.23 |
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