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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(TG-RET/CCDC6)42Cled
transgene insertion 42, Catherine Ledent
MGI:5569727
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
tg1
Tg(TG-RET/CCDC6)42Cled/0 involves: FVB/N MGI:5897617


Genotype
MGI:5897617
tg1
Allelic
Composition
Tg(TG-RET/CCDC6)42Cled/0
Genetic
Background
involves: FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
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See publication links below for author information.
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body
• dwarfism
• T4 supplementation corrects the dwarfism

endocrine/exocrine glands
• pituitary glands have marked hyperplasia of thyrotrophs
• 90% of cells in the pars distalis are thyrotrophs
• pituitary glands have marked hypertrophy of thyrotrophs
• large and irregular thyroid follicles with little colloid are seen at E16.5 and at E18.5
• increase in proliferation rate of thyroid follicular cells at E16.5 and 2-3 weeks of age, although proliferation in the thyroid decreases with age
• all mice exhibit bilateral thyroid tumors by 4 days of age (J:55883)
• thyroid tumors tend to arise from the central portions of the thyroid lobes with peripheral areas frequently containing irregular, dilated follicles (J:55883)
• administration of exogenous T4 delays thyroid tumor development (J:55883)
• all mice develop bilateral thyroid carcinomas similar to human papillary thyroid carcinomas as early as 1 month of age (J:93679)
• intrathryoidal and periglandulal invasion is seen in all mice (J:93679)
• pregnant dams intraperitoneally injected with radioiodide show reduced iodine concentrating activity of thyroid glands at E18
• radioiodide concentrating activity is reduced in the thyroid glands at all ages
• total iodide uptake activity in the thyroid glands is 30-fold lower than in controls
• mice supplemented with T4, when serum T4 and TSH levels are comparable to controls, total iodide uptake activity in the thyroid gland is 7-fold lower than in controls
• congenital hypothyroidism in all mice (J:93679)

homeostasis/metabolism
• low serum thyroxine (T4) levels
• low serum triiodothyronine (T3) levels

neoplasm
• all mice exhibit bilateral thyroid tumors by 4 days of age (J:55883)
• thyroid tumors tend to arise from the central portions of the thyroid lobes with peripheral areas frequently containing irregular, dilated follicles (J:55883)
• administration of exogenous T4 delays thyroid tumor development (J:55883)
• all mice develop bilateral thyroid carcinomas similar to human papillary thyroid carcinomas as early as 1 month of age (J:93679)
• intrathryoidal and periglandulal invasion is seen in all mice (J:93679)

nervous system
• pituitary glands have marked hyperplasia of thyrotrophs
• 90% of cells in the pars distalis are thyrotrophs
• pituitary glands have marked hypertrophy of thyrotrophs

renal/urinary system
• males develop penile prolapse (paraphimosis) with edema and ulceration at about 45 days of age

reproductive system
• males develop penile prolapse (paraphimosis) with edema and ulceration at about 45 days of age

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
papillary thyroid carcinoma DOID:3969 OMIM:188550
J:55883 , J:93679





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last database update
11/05/2024
MGI 6.24
The Jackson Laboratory