About   Help   FAQ
Phenotypes Associated with This Genotype
Genotype
MGI:5637537
Allelic
Composition
Trhrtm1Bau/Trhrtm1Bau
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Trhrtm1Bau mutation (0 available); any Trhr mutation (33 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
endocrine/exocrine glands
• mice exhibit central hypothyroidism

growth/size/body
• in hypothyroid mutants
• fasting-induced weight loss is higher in hypothyroid and euthyroid mutants than in wild-type mice

homeostasis/metabolism
• hypothyroid mutants under fasting conditions show only a marginal elevation in serum ghrelin levels compared to fasting wild-type mice or euthyroid mutants
• acylated ghrelin levels in the serum are similar in hypothyroid and euthyroid mutants as in wild-type mice under feeding conditions
• the fasting-induced rise in acylated ghrelin that is seen in wild-type mice is diminished in hypothyroid and in euthyroid mutants
• hypothyroid mutants show elevated total ghrelin serum levels under feeding conditions compared to euthyroid mutants and wild-type mice
• mice rendered euthyroid by thyroid hormone treatment before fasting show lower serum thyroid hormone levels
• however, serum thyroid hormone levels do not change in hypothyroid mutants upon fasting
• approximate 50% reduction in serum T3 and T4 concentrations
• approximate 50% reduction in serum T3 and T4 concentrations
• increase in oxygen consumption under conditions of ad libitum food accessibility
• hypothyroid mutants display similar oxygen consumption and locomotor activity values under fasting and feeding conditions in the first hours of the dark period unlike wild-type mice which show a mild reduction in oxygen consumption and lower locomotor activity under food deprivation conditions
• however, oxygen consumption and locomotor activity decline in the second half of the fasting period as in wild-type mice

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
congenital hypothyroidism DOID:0050328 OMIM:PS275200
J:220755


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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
12/10/2024
MGI 6.24
The Jackson Laboratory