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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Trim37Gt(RRO307)Byg
gene trap RRO307, BayGenomics
MGI:4329141
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Trim37Gt(RRO307)Byg/Trim37Gt(RRO307)Byg B6J.129P2-Trim37Gt(RRO307)Byg MGI:5789948


Genotype
MGI:5789948
hm1
Allelic
Composition
Trim37Gt(RRO307)Byg/Trim37Gt(RRO307)Byg
Genetic
Background
B6J.129P2-Trim37Gt(RRO307)Byg
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Trim37Gt(RRO307)Byg mutation (0 available); any Trim37 mutation (40 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• 1 female presented with primitive neuroendocrine tumor in the liver, pancreas, and thymus at 21 months of age

mortality/aging
• spontaneous deaths in 9 of 59 mice and increasing problems in well-being (including illness, weight loss, dental problems, visible tumors, and dermatitis) leading to euthanasia in 13 of 59 of mice at 18 months of age

reproductive system
• significantly reduced oocyte number in ovaries at P30
• absence of female germ cells at 6 months of age
• degeneration of male germ cells starting at P13
• total absence of male germ cells at 1 month of age
• absence of female germ cells at 6 months of age
• hilus cell hyperplasia in adult female mice
• ovarian lipid cell hyperplasia in some females at 6 months of age
• ovarian Sertoli cell tumors in 14 of 204 females at 14-22 months of age
• ovarian cysts in some females at 6 months of age
• progressive neutral fat accumulation in and around Leydig cells starting at 1 month of age, with excessive lipid accumulation evident at 18 months
• Leydig cell hyperplasia starting at P13 and increasing with age
• histological evidence of testicular (germ cell) degeneration as early as P13
• hypogonadism in >75 % of mice
• testis size is ~30% of that in control mice at >6 months of age
• both males and females are infertile
• females are able to become pregnant at the age of 6 weeks but older females are infertile
• males fail to reproduce at any age from postnatal week 6 onwards

growth/size/body
• enlarged pancreas in about one third of mice after 12 months of age
• ovarian cysts in some females at 6 months of age
• up to 20% weight loss in about one third of mice after 12 months of age
• males start losing weight at 6 months and females after 12 months of age
• however, early weight development is normal in both sexes
• tendency towards enlarged relative liver size, with pronounced hepatomegaly in a subset of female mice at 22-24 months of age
• however, hepatomegaly is infrequent at 18 months of age and no evidence of hepatic peliosis is observed
• splenomegaly in about one third of mice after 12 months of age

craniofacial
• sagittal skull width is 9.6 +/- 0.1 mm versus 9.8 +/- 0.1 mm in control mice
• coronal skull width 13.7 +/- 0.2 mm versus 14.0 +/- 0.2 mm in control mice
• significantly smaller than normal skull size at 6 months of age
• however, lengths of long bones (humeri, ulnae and femurs) are normal

endocrine/exocrine glands
• enlargement of pancreas with a granular appearance in about one third of mice after 12 months of age
• enlarged pancreas in about one third of mice after 12 months of age
• hilus cell hyperplasia in adult female mice
• ovarian lipid cell hyperplasia in some females at 6 months of age
• ovarian Sertoli cell tumors in 14 of 204 females at 14-22 months of age
• ovarian cysts in some females at 6 months of age
• progressive neutral fat accumulation in and around Leydig cells starting at 1 month of age, with excessive lipid accumulation evident at 18 months
• Leydig cell hyperplasia starting at P13 and increasing with age
• testis size is ~30% of that in control mice at >6 months of age
• histological evidence of testicular (germ cell) degeneration as early as P13

cardiovascular system
• sinusoidal dilatation at 22-24 months of age
• at 6 months of age, most mice exhibit more trabeculated ventricular walls relative to wild-type controls
• H&E staining of heart sections revealed myocardial hypertrabeculation at 6 months of age
• endothelial (anti-CD34) immunostaining) detected in trabeculations of the ventricular wall indicates non-compaction cardiomyopathy

liver/biliary system
• H&E staining of liver sections at 1-, 4-, 6- and 18 months of age shows progressive vacuolization of the liver
• sinusoidal dilatation at 22-24 months of age
• tendency towards enlarged relative liver size, with pronounced hepatomegaly in a subset of female mice at 22-24 months of age
• however, hepatomegaly is infrequent at 18 months of age and no evidence of hepatic peliosis is observed
• neutral lipid accumulation in liver (mostly triacylglycerols) starting at ~4-6 months of age, with both staining intensity and lipid droplet size increasing with age
• lipid accumulation in liver is highly variable and more prominent in females than in males
• fatty liver in about one third of mice after 12 months of age

homeostasis/metabolism
• after 24-h fasting, adult (6-month-old) male mice show increased fasting blood glucose levels
• increased FSH levels in male mice at 4 months of age
• however, testosterone levels remain normal
• increased LH levels in male mice at 4 months of age
• after 24-h fasting, adult (6-month-old) male mice display low fasting serum insulin levels
• however, number, size and distribution of pancreatic beta-islets is normal
• ascites in about one third of mice after 12 months of age
• reduced respiratory exchange ratio (RER) in 20-month-old mice fed a fat-enriched Western diet since weaning
• neutral lipid accumulation in liver (mostly triacylglycerols) starting at ~4-6 months of age, with both staining intensity and lipid droplet size increasing with age
• lipid accumulation in liver is highly variable and more prominent in females than in males

immune system
• splenomegaly in about one third of mice after 12 months of age

neoplasm
• primitive neuroendocrine tumors, lymphomas, and neuroendocrine carcinomas only occasionally seen
• 2 of 204 mice (females) presented with multiple tumors of the same type in different locations of the body
• ovarian Sertoli cell tumors in 14 of 204 females at 14-22 months of age
• 1 female presented with lymphoma in the lymph nodes, ovaries, and thymus, with distinct tumors in the area of the abdomen at 15 months of age
• 1 male presented with lymphoma in the lymph nodes at 18 months of age
• 1 female presented with primitive neuroendocrine tumor in the liver, pancreas, and thymus at 21 months of age
• 1 female presented with neuroendocrine carcinoma of the thymus at 14 months of age

hematopoietic system
• splenomegaly in about one third of mice after 12 months of age

behavior/neurological
• reduced water consumption in 20-month-old mice fed a fat-enriched Western diet since weaning
• reduced food intake in 20-month-old male mice fed a fat-enriched Western diet since weaning
• reduced mobility in about one third of mice after 12 months of age
• lower physical activity in 20-month-old mice fed a fat-enriched Western diet since weaning

muscle
• at 6 months of age, most mice exhibit more trabeculated ventricular walls relative to wild-type controls
• H&E staining of heart sections revealed myocardial hypertrabeculation at 6 months of age
• endothelial (anti-CD34) immunostaining) detected in trabeculations of the ventricular wall indicates non-compaction cardiomyopathy

skeleton
• sagittal skull width is 9.6 +/- 0.1 mm versus 9.8 +/- 0.1 mm in control mice
• coronal skull width 13.7 +/- 0.2 mm versus 14.0 +/- 0.2 mm in control mice
• significantly smaller than normal skull size at 6 months of age
• however, lengths of long bones (humeri, ulnae and femurs) are normal

cellular
N
• normal number, structure and distribution of liver peroxisomes relative to control mice
• significantly reduced oocyte number in ovaries at P30
• absence of female germ cells at 6 months of age
• degeneration of male germ cells starting at P13
• total absence of male germ cells at 1 month of age
• absence of female germ cells at 6 months of age

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
mulibrey nanism DOID:0050436 OMIM:253250
J:232482





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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory