|
Symbol Name ID |
Pxdn
peroxidasin MGI:1916925 |
| Darker colors indicate more annotations |
| Human Phenotypes | Anterior synechiae of the anterior chamber |
Microcornea |
Corneal opacity |
Sclerocornea |
Cataract |
Iris coloboma |
Ocular anterior segment dysgenesis |
Buphthalmos |
Microphthalmia |
Ocular hypertension |
Reduced visual acuity |
| Disease(s) Associated with PXDN | |||||||||||
| anterior segment dysgenesis 7 |
| Mouse Phenotypes | eye inflammation |
decreased retina ganglion cell number |
abnormal optic nerve morphology |
optic nerve hypoplasia |
abnormal anterior eye segment morphology |
abnormal iridocorneal angle |
ciliary body hypoplasia |
abnormal iris morphology |
iris hypoplasia |
decreased corneal epithelium thickness |
abnormal corneal stroma morphology |
increased corneal stroma thickness |
corneal opacity |
corneal-lenticular stalk |
fused cornea and lens |
abnormal eye anterior chamber morphology |
decreased eye anterior chamber depth |
absent eye anterior chamber |
abnormal eye posterior chamber morphology |
ruptured lens capsule |
abnormal lens development |
abnormal lens epithelium morphology |
abnormal lens fiber morphology |
disorganized secondary lens fibers |
small lens |
microphthalmia |
abnormal retina morphology |
abnormal retina inner limiting membrane morphology |
retina fold |
retina gliosis |
vitreous body deposition |
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| Availability | Mouse Genotype | |||||||||||||||||||||||||||||||
| Pxdnmhdakta048/Pxdnmhdakta048 | ||||||||||||||||||||||||||||||||
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 04/16/2024 MGI 6.23 |
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