About   Help   FAQ
Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Brs3tm1Hoh
targeted mutation 1, Hiroko Ohki-Hamazaki
MGI:2387858
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Brs3tm1Hoh/Brs3tm1Hoh involves: 129P2/OlaHsd * C57BL/6J MGI:2658811


Genotype
MGI:2658811
hm1
Allelic
Composition
Brs3tm1Hoh/Brs3tm1Hoh
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Brs3tm1Hoh mutation (0 available); any Brs3 mutation (14 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
adipose tissue
• at 27-34 weeks, mutants exhibited an increased amount of white adipose tissue mass

behavior/neurological
N
• when placed in a cage, mutants did not display a reduction in activity compared to controls during the test period (1 hour)
• mutants showed normal activity levels both during light and dark periods over a 3-week observation period
• at 10-12 weeks, food intake was similar to that of wild-type, but water intake was reduced
• at 20-24 weeks, while obesity progressed, mutants ingested ~9% more calories than wild-type
• in addition to hyperphagia, mutants exhibited increased feed efficiency: as a result, they displayed a slower rate of weight loss when food was restricted

cardiovascular system
• at 40 weeks of age, mutants showed increases of 13% and 27% in systolic and diastolic blood pressure, respectively

growth/size/body
• beginning at ~16 weeks, mutants (F2 generation) showed a significantly greater weight gain relative to wild-type
• mild obesity was preceded by a reduced metabolic rate

homeostasis/metabolism
N
• mutants showed no defects in body temperature regulation, and displayed normal non-shivering brown-fat thermogenesis
• the level of circulating leptin was elevated by 38% at 10 weeks; at 21-22 weeks it reached a concentration 5x higher than that measured in wild-type
• in mutants, the secretion of growth hormone was diminished by 46%; in contrast, blood contents of thyroid hormone and glucagon appeared unaffected
• at 6-7 weeks, mutants consumed 11% less oxygen than wild-type in the resting state
• following oral glucose administration, 26-week-old mutants showed higher levels of blood glucose and insulin relative to wild-type
• following insulin injection, mutants were unable to clear glucose as efficiently as wild-type
• following a 24 hr fasting period, the blood glucose, cholesterol and triacyl glycerol levels were normal; however, at 23 weeks, the insulin level was elevated significantly relative to wild-type
• mutants became obese despite the elevated plasma leptin level, suggesting reduced leptin sensitivity





Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
10/29/2024
MGI 6.24
The Jackson Laboratory