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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Ahrtm3.1Bra
targeted mutation 3.1, Christopher A Bradfield
MGI:3612477
Summary 4 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Ahrtm3.1Bra/Ahrtm3.1Bra
Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
B6.Cg-Ahrtm3.1Bra Speer6-ps1Tg(Alb-cre)21Mgn MGI:3613531
cn2
Ahrtm3.1Bra/Ahrtm3.1Bra
Tg(Tek-cre)12Flv/0
B6.Cg-Ahrtm3.1Bra Tg(Tek-cre)12Flv MGI:3613532
cn3
Ahrtm3.1Bra/Ahrtm3.1Bra
Tg(Nes-cre)1Kln/0
involves: 129/Sv * C57BL/6 * SJL MGI:6451067
cn4
Ahrtm3.1Bra/Ahrtm3.1Bra
Tg(Six3-cre)69Frty/0
Not Specified MGI:6199668


Genotype
MGI:3613531
cn1
Allelic
Composition
Ahrtm3.1Bra/Ahrtm3.1Bra
Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
Genetic
Background
B6.Cg-Ahrtm3.1Bra Speer6-ps1Tg(Alb-cre)21Mgn
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ahrtm3.1Bra mutation (1 available); any Ahr mutation (112 available)
Speer6-ps1Tg(Alb-cre)21Mgn mutation (6 available); any Speer6-ps1 mutation (4 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
N
• no defect in the closure of the ductus venosus is seen unlike in mice homozygous for Ahrtm3Bra

homeostasis/metabolism
• exposure to 100 ug 2,3,7,8-tetrachlorodibenzo-p-dioxin failed to induce hepatomegaly, or Cyp1a2 expression, only weakly induced Cyp1a1 expression, partially induced Cyp1b1 expression, and resulted in significantly less liver damage compared to homozygous mice lacking the cre transgene
• however, exposure to 100 ug 2,3,7,8-tetrachlorodibenzo-p-dioxin did induce thymic involution similar to homozygous mice lacking the cre transgene




Genotype
MGI:3613532
cn2
Allelic
Composition
Ahrtm3.1Bra/Ahrtm3.1Bra
Tg(Tek-cre)12Flv/0
Genetic
Background
B6.Cg-Ahrtm3.1Bra Tg(Tek-cre)12Flv
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ahrtm3.1Bra mutation (1 available); any Ahr mutation (112 available)
Tg(Tek-cre)12Flv mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• 18 of 22 mutants retain a patent ductus venosus as adults

cellular
• 18 of 22 mutants retain a patent ductus venosus as adults




Genotype
MGI:6451067
cn3
Allelic
Composition
Ahrtm3.1Bra/Ahrtm3.1Bra
Tg(Nes-cre)1Kln/0
Genetic
Background
involves: 129/Sv * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ahrtm3.1Bra mutation (1 available); any Ahr mutation (112 available)
Tg(Nes-cre)1Kln mutation (4 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• increased proliferative neural progenitor cells (NPCs) at the ipsilesional neurogenic zones after MCAO
• decreased GFAP-positive astrogliosis and Iba1-positive microgliosis at the peri-infarct cortex after MCAO
• shorter time to remove adhesive from affected forepaws in adhesive removal test, successfully retrieved more pasta pieces in skilled reaching task and explored novel object more than familiar object in novel object recognition test for non-spatial working memory, at 48 h and 7 days after middle cerebral artery occlusion (MCAO)
• decreased GFAP-positive astrogliosis and Iba1-positive microgliosis at the peri-infarct cortex after MCAO
• increased proliferative neural progenitor cells (NPCs) at the ipsilesional neurogenic zones after MCAO

homeostasis/metabolism
• increased proliferative neural progenitor cells (NPCs) at the ipsilesional neurogenic zones after MCAO
• decreased GFAP-positive astrogliosis and Iba1-positive microgliosis at the peri-infarct cortex after MCAO
• shorter time to remove adhesive from affected forepaws in adhesive removal test, successfully retrieved more pasta pieces in skilled reaching task and explored novel object more than familiar object in novel object recognition test for non-spatial working memory, at 48 h and 7 days after middle cerebral artery occlusion (MCAO)




Genotype
MGI:6199668
cn4
Allelic
Composition
Ahrtm3.1Bra/Ahrtm3.1Bra
Tg(Six3-cre)69Frty/0
Genetic
Background
Not Specified
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ahrtm3.1Bra mutation (1 available); any Ahr mutation (112 available)
Tg(Six3-cre)69Frty mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
• increased expression of proapoptotic protein Ddit3
• according to TUNEL assay
• thinner at age 18 months
• thinner at age 18 months
• reduced number of photoreceptor cells per row in outer nuclear layer (ONL) at age 18 months
• reduced number of photoreceptor cells per row at age 18 months
• reduced number of photoreceptor cells outer nuclear layer (ONL) per row at age 18 months
• thinner outer segment at age 18 months
• inner nuclear layer (INL) at age 18 months
• decreased scotopic responses at age 12 months: around 30 % reduction in b-wave and around 15 % reduction in a-wave mean amplitude at 0 and 1 log cd.s/m2 light intensity

nervous system
• thinner at age 18 months
• thinner at age 18 months
• reduced number of photoreceptor cells per row in outer nuclear layer (ONL) at age 18 months

cellular
• increased expression of proapoptotic protein Ddit3
• according to TUNEL assay





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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory