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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Mc4rtm1.1Fbz
targeted mutation 1.1, Florian Bolze
MGI:5703936
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Mc4rtm1.1Fbz/Mc4rtm1.1Fbz involves: 129S4/SvJae * C57BL/6 * C57BL/6J * C57BL/6NTac MGI:5707333
ht2
Mc4rtm1.1Fbz/Mc4r+ involves: 129S4/SvJae * C57BL/6 * C57BL/6J * C57BL/6NTac MGI:5707334


Genotype
MGI:5707333
hm1
Allelic
Composition
Mc4rtm1.1Fbz/Mc4rtm1.1Fbz
Genetic
Background
involves: 129S4/SvJae * C57BL/6 * C57BL/6J * C57BL/6NTac
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mc4rtm1.1Fbz mutation (0 available); any Mc4r mutation (48 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body
• when singly housed under SPF conditions, homozygotes of both sexes show reduced abdominal lean mass relative to wild -type controls
• at 25-28 weeks of age, only male homozygotes show a higher abdominal lean mass than age-matched heterozygous and wild-type littermates, indicating a sex-specific difference in lean mass
• at ~6-7 weeks of age, homozygotes of both sexes are obviously heavier than wild-type controls
• homozygotes become obese by 9 weeks of age
• at >6 months of age, male and female homozygotes weigh 70% and 100% more, respectively, than wild-type controls
• obesity was not ameliorated during a 7-day gentamicin treatment of male homozygotes at the age of 36 weeks
• similarly, no reduction of obesity was observed during a 19-day amikacin treatment of female homozygotes at the age of 42 weeks
• at ~20 weeks of age, homozygotes of both sexes show a ~10% increase in snout-to-anus distance relative to wild -type controls

behavior/neurological
• at ~20 weeks of age, homozygotes of both sexes display hyperphagia resulting in an increased energy intake and energy assimilation (defined as the amount of energy resorbed by the intestine epithelium)
• however, assimilation efficiency is unaffected, indicating normal nutrient resorption

adipose tissue
• analysis of abdominal body composition of dead mice at 25-28 weeks of age revealed that increased body weight is mainly due to an increase in visceral fat mass

homeostasis/metabolism
• at 9 weeks of age, obese homozygotes of both sexes display significantly increased daily energy expenditure relative to wild-type controls, as shown by indirect calorimetry
• however, no difference in metabolic rate is noted in young pre-obese homozygotes at 6 weeks of age
• respiratory quotient is normal
• at ~20 weeks of age, homozygotes of both sexes display impaired glucose tolerance
• males are more affected than females




Genotype
MGI:5707334
ht2
Allelic
Composition
Mc4rtm1.1Fbz/Mc4r+
Genetic
Background
involves: 129S4/SvJae * C57BL/6 * C57BL/6J * C57BL/6NTac
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mc4rtm1.1Fbz mutation (0 available); any Mc4r mutation (48 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body
• at ~6-7 weeks of age, heterozygotes show an increase in body weight that is intermediate between that of homozygous mutant and wild-type littermates
• at ~20 weeks of age, heterozygotes of both sexes show a ~5% increase in snout-to-anus distance relative to wild-type controls

adipose tissue
• analysis of abdominal body composition of dead mice at 25-28 weeks of age revealed that heterozygotes show a gain in fat mass intermediate to that observed in homozygous mutant and wild-type littermates

homeostasis/metabolism
N
• heterozygotes display normal energy intake and assimilation relative to wild-type controls





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