|
Symbol Name ID |
Myoc
myocilin MGI:1202864 |
Excel File
| Allelic Composition Genetic Background |
Annotated Term | Reference |
| Myoctm1.1Rjo/Myoctm1.1Rjo involves: 129S7/SvEvBrd * C57BL/6 |
no abnormal phenotype detected | J:72628 |
| Myoctm1Rjo/Myoctm1Rjo either: 129S7/SvEvBrd or (involves: 129S7/SvEvBrd * C57BL/6) |
no abnormal phenotype detected | J:72628 |
| Myoctm2.1Rjo/Myoctm2.1Rjo involves: 129S7/SvEvBrd * C57BL/6J |
abnormal intraocular pressure | J:115971 |
| normal vision/eye phenotype | J:115971 | |
| Tg(Myoc*Y423H)#Sit/0 B6.FVB-Tg(Myoc*Y423H)#Sit |
abnormal canal of Schlemm morphology | J:116124 |
| abnormal retina inner plexiform layer morphology | J:116124 | |
| abnormal retina neuronal layer morphology | J:116124 | |
| abnormal trabecular meshwork morphology | J:116124 | |
| astrocytosis | J:116124 | |
| axon degeneration | J:116124 | |
| ocular hypertension | J:116124 | |
| optic nerve degeneration | J:116124 | |
| retina ganglion cell degeneration | J:116124 |
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 09/08/2026 MGI 6.24 |
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