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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Hrh1tm1Wtn
targeted mutation 1, Takeshi Watanabe
MGI:2182945
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Hrh1tm1Wtn/Hrh1tm1Wtn B6.129P2-Hrh1tm1Wtn MGI:3761138
hm2
Hrh1tm1Wtn/Hrh1tm1Wtn involves: 129P2/OlaHsd * C57BL/6 MGI:3761125


Genotype
MGI:3761138
hm1
Allelic
Composition
Hrh1tm1Wtn/Hrh1tm1Wtn
Genetic
Background
B6.129P2-Hrh1tm1Wtn
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Hrh1tm1Wtn mutation (4 available); any Hrh1 mutation (35 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
adipose tissue
• the amount of brown adipose tissue at 48 weeks of age is increased relative to in wild-type mice
• insulin levels during a 4 week feeding schedule are lower than in mice fed ad libitum
• however, the levels of brown adipose tissue at 12 weeks of age is normal
• at 28 weeks of age, white adipose tissue is increased by 23%, 48% and 40% in the epididymmal, mesenteric and retroperitoneal fat pads, respectively, compared to wild-type mice
• unlike in wild-type mice, intraperitoneal administration of the histamine agonist methyl(2[2-pyridyl]ethyl)amine dyhydrochloride (1 ug/g for 7 days) results in decreased in adiposity
• adipocytes in the epididymal white adipose tissue are larger than in wild-type mice at 48 weeks of age
• however, adipocyte size at 12 weeks of age is normal

muscle
• mice exhibit 20% more triglycerides in skeletal muscle compared to wild-type mice

homeostasis/metabolism
• at 48 weeks of age, serum insulin levels are increased relative to in wild-type mice
• however, at 12 weeks of age serum insulin levels are normal
• at 48 weeks of age, leptin levels are increased by 66% compared to in wild-type mice
• however, at 12 weeks of age leptin levels are normal
• at 48 weeks of age, free fatty acid levels are increased relative to in wild-type mice
• however, at 12 weeks of age free fatty acid levels are normal
• mice exhibit 45% more triglycerides in the liver compared to wild-type mice
• mice exhibit 20% more triglycerides in skeletal muscle compared to wild-type mice
• following intracerebroventricular administration of 0.5 ug leptin or intraperitoneal injection of 50 ug of leptin, mice exhibit a smaller decrease in food consumption and body mass relative to wild-type

behavior/neurological
• at 48 weeks, the ratio of food consumed in the light versus dark phase is smaller than in wild-type mice
• unlike in wild-type mice, intraperitoneal administration of the histamine agonist methyl(2[2-pyridyl]ethyl)amine dyhydrochloride (1 ug/g for 7 days) results in decreased food intake
• however, intracerebroventricular administration of methyl(2[2-pyridyl]ethyl)amine dyhydrochloride has no effect on mice
• at 48 weeks of age, mice consume slightly more food than wild-type mice
• however, at 12 weeks of age food consumption is normal

growth/size/body
• during 4 week on a feeding schedule, mice fail to gain weight as do wild-type mice despite equivalent food consumption
• unlike in wild-type mice, intraperitoneal administration of the histamine agonist methyl(2[2-pyridyl]ethyl)amine dyhydrochloride (1 ug/g for 7 days) results in decreased body mass
• however, intracerebroventricular administration of methyl(2[2-pyridyl]ethyl)amine dyhydrochloride has no effect on mice
• after 28 weeks of age mice exhibit increased body mass relative to wild-type mice

immune system
• following ovalbumin challenge, IgG1, IgG2a and IgG2b levels are increased relative to similarly treated wild-type mice
• following ovalbumin challenge, IgM levels are increased relative to similarly treated wild-type mice
• antigen stimulation of splenocytes results in the production of less interferon-gamma compared to in similarly treated wild-type mice
• antigen stimulation of splenocytes results in the production of less IL-13 compared to in similarly treated wild-type mice
• antigen stimulation of splenocytes results in the production of less IL-5 compared to in similarly treated wild-type mice
• following challenge with ovalbumin, mice fail to develop lung inflammation as do wild-type mice with fewer eosinophils and lymphocytes detected in the bronchoalveolar lavage
• however, mice exhibit normal B cell immune responses and inhalation of IL-4 or IL-13 induces lung inflammation

liver/biliary system
• mice exhibit 45% more triglycerides in the liver compared to wild-type mice

hematopoietic system
• following ovalbumin challenge, IgG1, IgG2a and IgG2b levels are increased relative to similarly treated wild-type mice
• following ovalbumin challenge, IgM levels are increased relative to similarly treated wild-type mice




Genotype
MGI:3761125
hm2
Allelic
Composition
Hrh1tm1Wtn/Hrh1tm1Wtn
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Hrh1tm1Wtn mutation (4 available); any Hrh1 mutation (35 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• however, B cell proliferation in response to IL-4 alone or in combination with CD40LG or LPS is normal
• B cell proliferation in response to anti-IgM is reduced 3- to 4-fold compared to in wild-type mice
• T cell proliferation in response to anti-CD3-epsilon is reduced 5- to 8-fold compared to in wild-type mice
• T cell proliferation in response to ovalbmin is reduced 4- to 6-fold compared to in wild-type mice
• however, T cell proliferation in response to PHA is normal
• the number of CD5+ B220+ T cells is slightly decreased (21.0+/-8.6% compared to 39.5+/-9.1% in wild-type mice)
• IgG3 levels are slightly lower than in wild-type mice
• following challenge with ovalbumin, anti-ovalbumin IgG3 antibodies are lower than in similarly treated wild-type mice
• following stimulation with TNP-Ficoll, anti-TNP IgM antibodies are 9-fold lower than in similarly treated wild-type mice
• following challenge with ovalbumin, anti-ovalbumin IgM antibodies are lower than in similarly treated wild-type mice
• following in vitro stimulation with ovalbumin or anti-CD3 epsilon antibodies, cells produce less interferon-gamma than wild-type mice
• following in vitro stimulation with ovalbumin or anti-CD3 epsilon antibodies, cells produce less IL-2
• following in vitro stimulation with ovalbumin or anti-CD3 epsilon antibodies, cells produce more IL-4 than wild-type mice

behavior/neurological
• during passive avoidance testing, mice display more frequent urination and defecation and decreased movement compared to wild-type mice
• however, passive avoidance behavior is normal
• despite normal motor coordination, mice exhibit decreased ambulation and time of rearing for the first 30 minutes when placed in a new environment
• mice exhibit increased locomotor activity during early portions of the light phase and decreased ambulation during the dark phase of a 12 hours light 12 hour dark cycle relative to similarly treated wild-type mice
• the ratio of ambulation during the light phase to total ambulation during 24 hours is increased compared to in wild-type mice
• however, total ambulation during a 24 hours period is normal
• mice rear less when placed in a new environment compared to wild-type mice

hematopoietic system
• B cell proliferation in response to anti-IgM is reduced 3- to 4-fold compared to in wild-type mice
• however, B cell proliferation in response to IL-4 alone or in combination with CD40LG or LPS is normal
• T cell proliferation in response to anti-CD3-epsilon is reduced 5- to 8-fold compared to in wild-type mice
• T cell proliferation in response to ovalbmin is reduced 4- to 6-fold compared to in wild-type mice
• however, T cell proliferation in response to PHA is normal
• the number of CD5+ B220+ T cells is slightly decreased (21.0+/-8.6% compared to 39.5+/-9.1% in wild-type mice)
• IgG3 levels are slightly lower than in wild-type mice
• following challenge with ovalbumin, anti-ovalbumin IgG3 antibodies are lower than in similarly treated wild-type mice
• following stimulation with TNP-Ficoll, anti-TNP IgM antibodies are 9-fold lower than in similarly treated wild-type mice
• following challenge with ovalbumin, anti-ovalbumin IgM antibodies are lower than in similarly treated wild-type mice

cellular
• B cell proliferation in response to anti-IgM is reduced 3- to 4-fold compared to in wild-type mice
• however, B cell proliferation in response to IL-4 alone or in combination with CD40LG or LPS is normal
• T cell proliferation in response to anti-CD3-epsilon is reduced 5- to 8-fold compared to in wild-type mice
• T cell proliferation in response to ovalbmin is reduced 4- to 6-fold compared to in wild-type mice
• however, T cell proliferation in response to PHA is normal





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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory