cellular
• some (about 5%) seminiferous tubules lack spermatogonia
|
• progressive germ cell depletion
|
• a 67% decrease in epididymal sperm concentration at 12 weeks of age
• despite the decrease in sperm concentration, males are fertile
|
• about 5% of seminiferous tubules contain a cohort of spermatocytes arrested in meiosis
|
mortality/aging
N |
• viable
|
liver/biliary system
• increased incidence in males at 1 year of age and all affected mice have multiple hepatocellular carcinomas
|
reproductive system
• some (about 5%) seminiferous tubules lack spermatogonia
|
• progressive germ cell depletion
|
• a 67% decrease in epididymal sperm concentration at 12 weeks of age
• despite the decrease in sperm concentration, males are fertile
|
• about 5% of seminiferous tubules contain a cohort of spermatocytes arrested in meiosis
|
• at 1 year of age
|
• some tubules show progressive germ cell depletion, lack spermatogonia or contain a cohort of spermatocytes arrested in meiosis
|
small testis
(
J:177420
)
• detected at puberty and the difference in size compared to controls increases over time
|
• most females are infertile
|
neoplasm
• all males develop tumors by 1 year of age
|
• at 1 year of age
|
• increased incidence in males at 1 year of age and all affected mice have multiple hepatocellular carcinomas
|
• tubulostromal adenomas
|
endocrine/exocrine glands
• at 1 year of age
|
• some tubules show progressive germ cell depletion, lack spermatogonia or contain a cohort of spermatocytes arrested in meiosis
|
small testis
(
J:177420
)
• detected at puberty and the difference in size compared to controls increases over time
|
growth/size/body
Mouse Models of Human Disease |
DO ID | OMIM ID(s) | Ref(s) | |
hepatocellular carcinoma | DOID:684 |
OMIM:114550 |
J:177420 |