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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Fam20bGt(GST_4283_D8)Lex
gene trap GST_4283_D8, Lexicon Genetics
MGI:5432371
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Fam20bGt(GST_4283_D8)Lex/Fam20bGt(GST_4283_D8)Lex involves: 129S5/SvEvBrd * C57BL/6 MGI:5432372


Genotype
MGI:5432372
hm1
Allelic
Composition
Fam20bGt(GST_4283_D8)Lex/Fam20bGt(GST_4283_D8)Lex
Genetic
Background
involves: 129S5/SvEvBrd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fam20bGt(GST_4283_D8)Lex mutation (0 available); any Fam20b mutation (29 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• only 2 homozygous embryos out of 29 present at E12.5
• multisystem organ hypoplasia and delayed development

embryo

growth/size/body

digestive/alimentary system
• organ hypoplasia and delayed development

liver/biliary system
• organ hypoplasia and delayed development

respiratory system
• organ hypoplasia and delayed development

skeleton
• organ hypoplasia and delayed development

vision/eye
• organ hypoplasia and delayed development





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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
11/12/2024
MGI 6.24
The Jackson Laboratory