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Phenotypes Associated with This Genotype
Genotype
MGI:4456447
Allelic
Composition
Tmed299J/Tmed299J
Genetic
Background
involves: C3HeB/FeJ * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tmed299J mutation (0 available); any Tmed2 mutation (7 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice do not survive embryogenesis
• some mice die prior to E9.5
• no mice are recovered at E11.5 and E12.5

embryo
• mice fail to turn by E9.5
• at E10.5, the caudal end of the embryo is reduced in size and consists of a small, malformed tail bud devoid of tissue unlike in wild-type mice
• at E9.5
• at E8.5, fewer than expected somites have formed when compared with wild-type mice
• at E9.5, 0 to 10 somites have formed compared with 20-22 in wild-type mice
• small and irregularly shaped at E9.5
• at E9.5
• bulbous at E9.5
• at E8.5 likely due to overall developmental delay

cardiovascular system
• 54% of mice exhibit irregular heart looping when compared with wild-type mice
• in 23% of mice
• in 10% of mice at E.9.5

limbs/digits/tail
• small and irregularly shaped at E9.5
• at E9.5

nervous system
• at E9.5

growth/size/body


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