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Phenotypes Associated with This Genotype
Genotype
MGI:3803670
Allelic
Composition
Wt1tm1Mlh/Wt1tm1Mlh
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Wt1tm1Mlh mutation (2 available); any Wt1 mutation (35 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• homozygotes are embryonic lethal
• 17% of embryos die by E12.5 and 71% of embryos die by E13.5

growth/size/body
• embryo size is reduced at E12.5 and E13.5 compared to age-matched control embryos

endocrine/exocrine glands
• adrenal primordia in E13.5 embryos are significantly smaller
• gonads are absent in all E13.5 embryos

embryo
• embryo size is reduced at E12.5 and E13.5 compared to age-matched control embryos

reproductive system
• gonads are absent in all E13.5 embryos

renal/urinary system
• E13.5 embryos fail to develop a metanephros

cardiovascular system
• cardiac dysplasia is noted in all embryos at E13.5
• both ventricles have poorly developing compact and trabecular myocardium in the free walls
• atrial cavaties are dilated with thickened epicardium
• other cardiac abnormalities noted in E13.5 embryos are hypoplastic myocardium, heart shape abnormalities with rounded apex, and improper epicardium and mesocardial attachment
• rounded heart apex
• pericardial hemorrhaging in about half the embryos

liver/biliary system
• the livers of E12.5 and E13.5 embryos are hypoplastic and deficient in lobation

muscle
• diaphragms are incompletely formed in all embryos at E12.5 with an increase in the dorsolateral gap
• E13.5 embyros have large openings between the pleural and peritoneal spaces

homeostasis/metabolism
• pericardial hemorrhaging in about half the embryos


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
01/28/2026
MGI 6.24
The Jackson Laboratory