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Phenotypes Associated with This Genotype
Genotype
MGI:3623225
Allelic
Composition
Trhtm1Mmt/Trhtm1Mmt
Genetic
Background
involves: C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Trhtm1Mmt mutation (0 available); any Trh mutation (25 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
endocrine/exocrine glands
• in 8 week old mutants, hypoplasia is observed in thrytrophs but not in other pituitary hormone-producing cells

homeostasis/metabolism
• in mutants by postnatal day 10, the level of thyroid hormone increases only by 3-fold from level at birth compared to a 6-fold increase in wild-type animals; levels at 21 days and 8 weeks are 28.3% and 50.3% of wild-type levels, respectively
• there is significantly decreased levels of TSH in the pituitary of homozygous mice

nervous system
• in 8 week old mutants, hypoplasia is observed in thrytrophs but not in other pituitary hormone-producing cells


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
03/31/2026
MGI 6.24
The Jackson Laboratory