Symbol Name ID |
Col4a3
collagen, type IV, alpha 3 MGI:104688 |
Darker colors indicate more annotations |
Human Phenotypes | Hypophosphatemia |
Azotemia |
Hematuria |
Microscopic hematuria |
Proteinuria |
Disease(s) Associated with COL4A3 | |||||
Alport syndrome | |||||
autosomal dominant Alport syndrome | |||||
autosomal recessive Alport syndrome | |||||
benign familial hematuria |
Mouse Phenotypes | increased circulating creatinine level |
increased blood urea nitrogen level |
decreased circulating amylase level |
uremia |
increased urine protein level |
albuminuria |
hematuria |
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Availability | Mouse Genotype | |||||||
Col4a3tm1b(EUCOMM)Wtsi/Col4a3tm1b(EUCOMM)Wtsi | ||||||||
Col4a3tm1Dec/Col4a3tm1Dec | ||||||||
Col4a3tm1Jhm/Col4a3tm1Jhm | ||||||||
Col4a3tm1.1Rkl/Col4a3+ |
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 07/05/2024 MGI 6.24 |
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