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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Akr1b1tm1.1Kgab
targeted mutation 1.1, Kenneth H Gabbay
MGI:5008171
Summary 2 genotypes


Genotype
MGI:5008184
hm1
Allelic
Composition
Akr1b1tm1.1Kgab/Akr1b1tm1.1Kgab
Genetic
Background
B6.Cg-Akr1b1tm1.1Kgab
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Akr1b1tm1.1Kgab mutation (0 available); any Akr1b1 mutation (27 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
homeostasis/metabolism
• male mice exhibit a decrease in liver and kidney ascorbate levels compared with wild-type mice




Genotype
MGI:5008183
cx2
Allelic
Composition
Akr1a1Gt(OST222400)Lex/Akr1a1Gt(OST222400)Lex
Akr1b1tm1.1Kgab/Akr1b1tm1.1Kgab
Genetic
Background
B6.Cg-Akr1a1Gt(OST222400)Lex Akr1b1tm1.1Kgab
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Akr1a1Gt(OST222400)Lex mutation (0 available); any Akr1a1 mutation (31 available)
Akr1b1tm1.1Kgab mutation (0 available); any Akr1b1 mutation (27 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

"Rachitic rosary" phenotype of Gulotm1Mae/Gulotm1Mae and Akr1b1tm1.1Kgab/Akr1b1tm1.1Kgab Akr1a1Gt(OST222400)Lex/Akr1a1Gt(OST222400)Lex bones

mortality/aging
• mice die at 8 to 10 weeks of age

skeleton
• newborn mice exhibit rapid onset of scurvy with ball-like swellings at the costochondral junction of the ribs resulting from hemorrhage and callus formation due to profound ascorbate deficiency





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last database update
10/29/2024
MGI 6.24
The Jackson Laboratory