Symbol Name ID |
Loxl1
lysyl oxidase-like 1 MGI:106096 |
Darker colors indicate more annotations |
Human Phenotypes | Iris hypoperfusion |
Retinal vein occlusion |
Pigment deposition in the trabecular meshwork |
Abnormal lens morphology |
Cataract |
Lens subluxation |
Phakodonesis |
Anisocoria |
Pseudoexfoliation |
Asymmetry of intraocular pressure |
Mydriasis |
Myopia |
Glaucoma |
Open angle glaucoma |
Disease(s) Associated with LOXL1 | ||||||||||||||
exfoliation syndrome | ||||||||||||||
primary open angle glaucoma |
Mouse Phenotypes | abnormal ciliary body morphology |
abnormal iris morphology |
abnormal eye anterior chamber morphology |
abnormal lens morphology |
abnormal lens fiber morphology |
anterior subcapsular cataract |
abnormal retina morphology |
abnormal intraocular pressure |
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Availability | Mouse Genotype | ||||||||
Loxl1tm1.1(KOMP)Vlcg/Loxl1tm1.1(KOMP)Vlcg | |||||||||
Loxl1tm1Tili/Loxl1tm1Tili | |||||||||
Tg(CRYBB1-Loxl1)1Erta/0 |
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 09/03/2024 MGI 6.24 |
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