pigmentation
• mutants closely resemble agouti mice or mice deficient in Pmoc1 or Mcr4
|
adipose tissue
• body fat is increased 2-fold, a disproportionate increase relative to the increase in body weight
|
behavior/neurological
polydipsia
(
J:93415
)
• mutants drink 65% more water than wild-type mice
|
polyphagia
(
J:93415
)
• mutants consume 60% more food than wild-type mice
|
endocrine/exocrine glands
• the number of beta cells does not increase from 4 to 8 weeks of age unlike in wild-type mice, however by 6 months beta cell numbers are normal as a result of proliferation of cells that escaped cre mediated recombination
|
growth/size/body
• increased body weight is seen after 4 weeks of age with mutants weighing 30% more than wild-type mice at 32 weeks of age
• lean mass and total body fat are increased relative to wild-type mice
|
• mutants are 10% longer than wild-type mice
|
homeostasis/metabolism
• fasting and random-fed glucose levels are elevated
|
• serum insulin is increased 2-fold, however pancreatic insulin levels were decreased more than 2-fold
• increased circulating insulin levels are also seen on a low fat diet
|
• serum leptin is increased 2-fold
|
• glucose intolerance is seen on a normal or low fat diet
|
• glucose clearance rates were decreased about 50% indicating peripheral insulin resistance
|
integument
• mutants closely resemble agouti mice or mice deficient in Pmoc1 or Mcr4
|
Mouse Models of Human Disease |
DO ID | OMIM ID(s) | Ref(s) | |
type 2 diabetes mellitus | DOID:9352 |
OMIM:125853 OMIM:601283 OMIM:601407 OMIM:603694 OMIM:608036 |
J:93415 |