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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Ireb2tm1.2Mwh
targeted mutation 1.2, Matthias W Hentze
MGI:3613524
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Ireb2tm1.2Mwh/Ireb2tm1.2Mwh involves: 129P2/OlaHsd * BALB/c * C57BL/6 * SJL MGI:3613561
cx2
Fbxl5Gt(OST386421)Lex/Fbxl5Gt(OST386421)Lex
Ireb2tm1.2Mwh/Ireb2tm1.2Mwh
involves: 129P2/OlaHsd * 129S5/SvEvBrd * C57BL/6 MGI:5470107


Genotype
MGI:3613561
hm1
Allelic
Composition
Ireb2tm1.2Mwh/Ireb2tm1.2Mwh
Genetic
Background
involves: 129P2/OlaHsd * BALB/c * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ireb2tm1.2Mwh mutation (0 available); any Ireb2 mutation (64 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hematopoietic system
• exhibit a minor but significant degree of erythropenia
• iron deficiency in the spleen

homeostasis/metabolism
• duodenal and hepatic iron accumulation is associated with increased ferritin L-chain expression and splenic iron deficiency is associated with decreased ferritin L-chain expression, however no differences in trans-ferrin staturation values
• iron loading of the duodenum
• however, no difference is seen in serum iron levels
• iron deficiency in the spleen
• increase in iron content in the liver

digestive/alimentary system
• iron loading of the duodenum
• however, no difference is seen in serum iron levels
• increase in iron content in the duodenum

immune system
• iron deficiency in the spleen

behavior/neurological
• locomotion is mildly affected, however do not display the neurodegenerative disorder seen in homozygous Ireb2tm1Roua mice

liver/biliary system
• increase in iron content in the liver




Genotype
MGI:5470107
cx2
Allelic
Composition
Fbxl5Gt(OST386421)Lex/Fbxl5Gt(OST386421)Lex
Ireb2tm1.2Mwh/Ireb2tm1.2Mwh
Genetic
Background
involves: 129P2/OlaHsd * 129S5/SvEvBrd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fbxl5Gt(OST386421)Lex mutation (0 available); any Fbxl5 mutation (45 available)
Ireb2tm1.2Mwh mutation (0 available); any Ireb2 mutation (64 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
N
• mice are viable

hematopoietic system





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