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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Klhl20Gt(XF202)Byg
gene trap XF202, BayGenomics
MGI:4127967
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Klhl20Gt(XF202)Byg/Klhl20Gt(XF202)Byg B6.129P2-Klhl20Gt(XF202)Byg MGI:5490898


Genotype
MGI:5490898
hm1
Allelic
Composition
Klhl20Gt(XF202)Byg/Klhl20Gt(XF202)Byg
Genetic
Background
B6.129P2-Klhl20Gt(XF202)Byg
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Klhl20Gt(XF202)Byg mutation (0 available); any Klhl20 mutation (36 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• fewer than expected mice are present at P28

vision/eye
N
• mice exhibit normal periocular lacrimal glands and embryonic development of the eye
• cornea are highly vascularized
• cornea are highly vascularized
• progressive epithelial metaplasia leading to corneal opacity
• hyperplasia with altered differentiation and severe keratinization
• starting in the third postnatal week

cardiovascular system
• cornea are highly vascularized
• cornea are highly vascularized

homeostasis/metabolism
• following mechanical injury (corneal abrasion), mice exhibit rapid development of corneal opacity with epithelial hyperplasia, stromal infiltrations and superficial keratinized cells unlike wild-type mice





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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
04/23/2024
MGI 6.23
The Jackson Laboratory