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Phenotype Image Detail
Image
Caption The Ppp1r13lwoe2/Ppp1r13lwoe2 eye phenotype at P28. Clinical evaluation of mutant eyes identified microphthalmia with corneal opacities and neovascularization (B) when compared with wild-type (WT) mice (A). In about 25% of mutant animals, unilateral or bilateral eyelid closure was noted (C). Histological analysis of mutant eyes (E) identified anterior segment abnormalities with extensive anterior synechia (arrow), corneal hypertrophy (arrowhead) and stromal vascularization. Histological analysis of closed mutant eyes (C) revealed aphakia with highly disorganized cornea, iris and retina (F). Histological analysis of adult mutant eyelids (H) identified absence of meibomian glands (arrow) whereas meibomian glands were present in age-matched WT eyelids (G) (asterisk). Scale bar in D-H = 100 um.
Copyright This image is from Toonen J, BMC Genet 2012;13():76, an open-access article, licensee BioMed Central Ltd. J:190557
Associated
Alleles
Symbol Name
Ppp1r13lwoe2 protein phosphatase 1, regulatory subunit 13 like; waved with open eyelids 2
Associated
Genotypes
Allelic Composition Genetic Background
Ppp1r13lwoe2/Ppp1r13lwoe2 involves: 129X1/SvJ * C57BL/6

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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
10/29/2024
MGI 6.24
The Jackson Laboratory