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Symbol
Name
ID
Loxl1
lysyl oxidase-like 1
MGI:106096
Phenotype annotations related to vision/eye
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
Availability Mouse Genotype
Loxl1tm1.1(KOMP)Vlcg/Loxl1tm1.1(KOMP)Vlcg
Loxl1tm1Tili/Loxl1tm1Tili
Tg(CRYBB1-Loxl1)1Erta/0

Contributing Projects:
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
The Jackson Laboratory