Symbol Name ID |
Col4a3
collagen, type IV, alpha 3 MGI:104688 |
Darker colors indicate more annotations |
Human Phenotypes | Sensorineural hearing impairment |
Hearing impairment |
Disease(s) Associated with COL4A3 | ||
Alport syndrome | ||
autosomal dominant Alport syndrome | ||
autosomal recessive Alport syndrome |
Mouse Phenotypes | abnormal stria vascularis vasculature morphology |
abnormal cochlear basement membrane morphology |
abnormal stria vascularis morphology |
abnormal strial marginal cell morphology |
abnormal membranous labyrinth morphology |
increased or absent threshold for auditory brainstem response |
sensorineural hearing loss |
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Availability | Mouse Genotype | |||||||
Col4a3tm1Dec/Col4a3tm1Dec | ||||||||
Col4a3tm1Jhm/Col4a3tm1Jhm |
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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