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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Slc29a3tm1Lex
targeted mutation 1, Lexicon Pharmaceuticals
MGI:5007332
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Slc29a3tm1Lex/Slc29a3tm1Lex involves: 129S5/SvEvBrd * C57BL/6 MGI:5312059


Genotype
MGI:5312059
hm1
Allelic
Composition
Slc29a3tm1Lex/Slc29a3tm1Lex
Genetic
Background
involves: 129S5/SvEvBrd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Slc29a3tm1Lex mutation (3 available); any Slc29a3 mutation (27 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging

immune system
N
• mice exhibit normal serum cytokine production
• by 8 weeks of age
• bone marrow cells exhibit increased granulocyte/macrophage colony formation compared with wild-type cells
• enlarged lysosomes containing undigested materials
• at 3 weeks of age, mice exhibit increased macrophage in the spleen compared with wild-type mice
• mice exhibit macrophage infiltration in multiple organs (including spleen, liver, pancreas and intestine) that worsens with age unlike in wild-type mice
• however, treatment with anti-macrophage colony-stimulating factor antibodies reduces splenic macrophage numbers
• macrophage proliferation and apoptosis are increased compared to in wild-type mice
• bone marrow-derived macrophage exhibit delayed degradation of apoptotic thymocytes and bacterial killing compared with wild-type cells
• bone marrow-derived macrophage challenged with exogenous apoptotic thymocytes exhibit an accumulation of adenosine in whole-cell extracts and purified lysosomal fraction
• however, bone marrow-derived macrophage exhibit normal phagocytosis and phagosome-lysosome fusion
• mice exhibit an increase in the absolute number of apoptotic macrophage compared with wild-type mice
• by 8 weeks of age
• L. monocytogenes-infected mice exhibit increased bacterial load and lethality compared with wild-type mice

hematopoietic system
• by 8 weeks of age
• bone marrow cells exhibit increased granulocyte/macrophage colony formation compared with wild-type cells
• extramedullary myelopoiesis without an acute inflammatory response due to defects in hematopoietic cells
• enlarged lysosomes containing undigested materials
• at 3 weeks of age, mice exhibit increased macrophage in the spleen compared with wild-type mice
• mice exhibit macrophage infiltration in multiple organs (including spleen, liver, pancreas and intestine) that worsens with age unlike in wild-type mice
• however, treatment with anti-macrophage colony-stimulating factor antibodies reduces splenic macrophage numbers
• macrophage proliferation and apoptosis are increased compared to in wild-type mice
• bone marrow-derived macrophage exhibit delayed degradation of apoptotic thymocytes and bacterial killing compared with wild-type cells
• bone marrow-derived macrophage challenged with exogenous apoptotic thymocytes exhibit an accumulation of adenosine in whole-cell extracts and purified lysosomal fraction
• however, bone marrow-derived macrophage exhibit normal phagocytosis and phagosome-lysosome fusion
• mice exhibit an increase in the absolute number of apoptotic macrophage compared with wild-type mice

cellular
• mice exhibit an increase in the absolute number of apoptotic macrophage compared with wild-type mice
• accumulation of adenosine in whole-cell extracts and purified lysosomes derived from splenic macrophage indicate impaired lysosomal nucleoside export

neoplasm
• in moribund mice
• however, treatment with anti-macrophage colony-stimulating factor antibodies partially rescues histocytic phenotype

growth/size/body
• by 8 weeks of age





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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
12/10/2024
MGI 6.24
The Jackson Laboratory