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Symbol Name ID |
Trpv4
transient receptor potential cation channel, subfamily V, member 4 MGI:1926945 |
| Darker colors indicate more annotations |
| Human Phenotypes | Opacification of the corneal stroma |
Cataract |
Oculomotor nerve palsy |
| Disease(s) Associated with TRPV4 | |||
| Charcot-Marie-Tooth disease axonal type 2C | |||
| metatropic dysplasia | |||
| spondyloepiphyseal dysplasia Maroteaux type |
| Mouse Phenotypes | abnormal trabecular meshwork morphology |
ocular hypertension |
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| Availability | Mouse Genotype | ||
| Trpv4tm1Rck/Trpv4tm1Rck | |||
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 04/30/2024 MGI 6.23 |
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