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Symbol
Name
ID
Col4a3
collagen, type IV, alpha 3
MGI:104688
Phenotype annotations related to homeostasis/metabolism
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
Availability Mouse Genotype
Col4a3tm1b(EUCOMM)Wtsi/Col4a3tm1b(EUCOMM)Wtsi
Col4a3tm1Dec/Col4a3tm1Dec
Col4a3tm1Jhm/Col4a3tm1Jhm
Col4a3tm1.1Rkl/Col4a3+

Contributing Projects:
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
04/09/2024
MGI 6.23
The Jackson Laboratory