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Phenotypes Associated with This Genotype
Genotype
MGI:3846169
Allelic
Composition
Hbatm1(HBA)Tow/Hbatm1(HBA)Tow
Hbbtm2(HBG1,HBD,HBB*)Ryan/Hbbtm2(HBG1,HBD,HBB*)Ryan
Genetic
Background
Not Specified
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Hbatm1(HBA)Tow mutation (3 available); any Hba mutation (10 available)
Hbbtm2(HBG1,HBD,HBB*)Ryan mutation (0 available); any Hbb mutation (47 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice have a median survival of 14 days after birth
• 65% of mice die between 11 and 18 days of age
• some mice die as early as 1 day after birth and one mouse of 17 survived into adulthood
• lethality can be rescued by transfusion

hematopoietic system
• spleen as a percentage of bodyweight is 14-fold greater than controls
• extramedullary hematopoiesis occurs in the spleen and liver
• large clusters of erythroblasts disrupt the architecture of the spleen and liver
• mice die of a lethal anemia
• anemia resembles beta thalassemia in humans
• anemia can be rescued by transfusion
• blood smears showed numerous damaged RBCs
• proerythroblast and early erythroblast numbers are increased in the bone marrow and spleen
• there is a higher ratio of early erythroblasts to late erythroblasts in both tissues
• increased levels of apoptosis occur to early and late erythroblasts in the bone marrow
• increased levels of apoptosis occur to late erythroblasts in the spleen
• red blood cell count is about 75% lower than controls
• hemoglobin content is decreased by more than 4-fold
• packed cell volume is decreased by almost two thirds
• red cell distribution width is greatly expanded
• visible in blood smears
• nucleated cells with polychromatophilia are visible in blood smears
• visible in blood smears
• percentage of reticulocytes in the blood is almost 72% compared to 3% in controls
• spleen architecture is disrupted by the presence of large numbers of erythroblasts

homeostasis/metabolism
• bilirubin levels are increased 150-fold in the blood

immune system
• spleen as a percentage of bodyweight is 14-fold greater than controls
• spleen architecture is disrupted by the presence of large numbers of erythroblasts

growth/size/body
• spleen as a percentage of bodyweight is 14-fold greater than controls

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
beta thalassemia DOID:12241 OMIM:613985
J:148521


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)
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last database update
04/09/2024
MGI 6.23
The Jackson Laboratory