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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Epb41tm1Cnby
targeted mutation 1, John G Conboy
MGI:2183903
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Epb41tm1Cnby/Epb41tm1Cnby involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ MGI:2449959


Genotype
MGI:2449959
hm1
Allelic
Composition
Epb41tm1Cnby/Epb41tm1Cnby
Genetic
Background
involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Epb41tm1Cnby mutation (0 available); any Epb41 mutation (95 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hematopoietic system
• 8 to 9-fold enlargement
• moderate
• mechanically compromised membrane; also increased osmotic fragility
• accelerated erythropoiesis in the spleen and liver
• 37% vs. 51% in wild-type mice
• red blood cells have a broader distribution of hemoglobin content that include cells with lower than normal hemoglobin content
• increased mean cell hemoglobin concentration
• decreased mean cell volume
• morphologic heterogeneity with many fragmented cells
• spherocytic morphology
• 11% vs. 2.5% in wild-type of reticulocytes in the blood
• iron deposition is reduced in spleen
• red pulp areas are expanded and filled with erythroid precursor cells

immune system
• 8 to 9-fold enlargement
• iron deposition is reduced in spleen
• red pulp areas are expanded and filled with erythroid precursor cells

homeostasis/metabolism
• iron deposition is reduced in spleen
• serum glutamic-oxaloacetic transaminase is elevated 2-3-fold
• creatine phosphokinase levels are increased about 2-fold in the blood
• extensive deposition of iron in the kidney proximal convoluted tubules
• increase in deposition of iron in the liver, indicating incrased red cell destruction

liver/biliary system
• increase in deposition of iron in the liver, indicating incrased red cell destruction

renal/urinary system
• extensive deposition of iron in the kidney proximal convoluted tubules

growth/size/body
• 8 to 9-fold enlargement

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
hereditary elliptocytosis DOID:2373 OMIM:130600
OMIM:611804
J:77852





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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
11/12/2024
MGI 6.24
The Jackson Laboratory