digestive/alimentary system
• rectal prolapse is seen at a median time of 11 weeks of age
|
• 88% of mutants with colonic inflammation exhibit colon tumors; majority of tumors are invasive adenocarcinomas
• mutants exhibit a higher tumor burden (3-4 tumors per colon on average) than single Il10 homozygotes (1 tumor per colon)
• tumors develop as early as 8-12 weeks of age
|
• mutants develop segmental, patchy colon inflammation with areas of healthy-appearing colon adjacent to areas of severe inflammation
• mutants exhibit higher total colonic inflammation at 5-6 weeks of age than single Il10 homozygotes and show fewer fields of no inflammation
• neutrophils are the dominant cellular infiltrate in the colon which are not seen in the single Il10 homozygote
• mutants develop progressive inflammatory bowel disease much earlier than single Il10 homozygotes
|
immune system
• mutants develop segmental, patchy colon inflammation with areas of healthy-appearing colon adjacent to areas of severe inflammation
• mutants exhibit higher total colonic inflammation at 5-6 weeks of age than single Il10 homozygotes and show fewer fields of no inflammation
• neutrophils are the dominant cellular infiltrate in the colon which are not seen in the single Il10 homozygote
• mutants develop progressive inflammatory bowel disease much earlier than single Il10 homozygotes
|
neoplasm
• 88% of mutants with colonic inflammation exhibit colon tumors; majority of tumors are invasive adenocarcinomas
• mutants exhibit a higher tumor burden (3-4 tumors per colon on average) than single Il10 homozygotes (1 tumor per colon)
• tumors develop as early as 8-12 weeks of age
|
Mouse Models of Human Disease |
DO ID | OMIM ID(s) | Ref(s) | |
colorectal cancer | DOID:9256 |
OMIM:114500 |
J:149347 | |
inflammatory bowel disease | DOID:0050589 |
OMIM:PS266600 |
J:149347 |