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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Elavl1tm1Thla
targeted mutation 1, Timothy Hla
MGI:4414853
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Elavl1tm1Thla/Elavl1tm1Thla
Gt(ROSA)26Sortm1(cre/ERT2)Alj/Gt(ROSA)26Sor+
involves: 129 MGI:4414940


Genotype
MGI:4414940
cn1
Allelic
Composition
Elavl1tm1Thla/Elavl1tm1Thla
Gt(ROSA)26Sortm1(cre/ERT2)Alj/Gt(ROSA)26Sor+
Genetic
Background
involves: 129
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Elavl1tm1Thla mutation (1 available); any Elavl1 mutation (43 available)
Gt(ROSA)26Sortm1(cre/ERT2)Alj mutation (0 available); any Gt(ROSA)26Sor mutation (993 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Cachexic phenotype of Elavl1tm1Thla/Elavl1tm1Thla Gt(ROSA)26Sortm1(cre/ERT2)Alj/Gt(ROSA)26Sor+ mice observed 4 days after tamoxifen administration

mortality/aging
• 10 days after tamoxifen treatment

immune system
• following tamoxifen treatment, double positive T cells in the thymus exhibit increased apoptosis and necrosis and decreased proliferation compared with T cells from Elavl1tm1Hela homozygotes
• following tamoxifen treatment
• 65% 4 days following tamoxifen treatment
• following tamoxifen treatment
• following tamoxifen treatment, myeloid cell numbers are decreased compared to in Elavl1tm1Hela homozygotes
• 4 days following tamoxifen treatment
• 2-fold following tamoxifen treatment
• following tamoxifen treatment
• following tamoxifen treatment, early B cells exhibit increased apoptosis and necrosis and decreased proliferation compared with B cells from Elavl1tm1Hela homozygotes
• following tamoxifen treatment, early B cells exhibit increased apoptosis and necrosis and decreased proliferation compared with B cells from Elavl1tm1Hela homozygotes
• following tamoxifen treatment

hematopoietic system
• following tamoxifen treatment, double positive T cells in the thymus exhibit increased apoptosis and necrosis and decreased proliferation compared with T cells from Elavl1tm1Hela homozygotes
• following tamoxifen treatment
• bone marrow from tamoxifen-treated mice exhibits decreased myeloerythroid colonies on methylcellulose compared with bone marrow from Elavl1tm1Hela homozygotes
• following tamoxifen treatment
• following tamoxifen treatment, total bone marrow cell numbers and bone marrow cellularity of immature cells are decreased compared to in Elavl1tm1Hela homozygotes
• following tamoxifen treatment
• 65% 4 days following tamoxifen treatment
• following tamoxifen treatment
• following tamoxifen treatment, myeloid cell numbers are decreased compared to in Elavl1tm1Hela homozygotes
• 4 days following tamoxifen treatment
• 2-fold following tamoxifen treatment
• following tamoxifen treatment
• following tamoxifen treatment, early B cells exhibit increased apoptosis and necrosis and decreased proliferation compared with B cells from Elavl1tm1Hela homozygotes
• following tamoxifen treatment, early B cells exhibit increased apoptosis and necrosis and decreased proliferation compared with B cells from Elavl1tm1Hela homozygotes

digestive/alimentary system
• 2 to 3 days following tamoxifen treatment, mice exhibit massive villus atrophy and disruption of the epithelial architecture unlike Elavl1tm1Hela homozygotes
• disrupted following tamoxifen treatment
• following tamoxifen treatment, goblet cells are lost unlike in Elavl1tm1Hela homozygotes
• following tamoxifen treatment, proliferation of crypt progenitor cells is decreased while apoptosis is increased unlike in Elavl1tm1Hela homozygotes
• following tamoxifen treatment, apoptosis of cells in the lamina propria and epithelial cells of the colon is increased compared to in Elavl1tm1Hela homozygotes
• 2 to 3 days following tamoxifen treatment, mice exhibit massive villus atrophy unlike Elavl1tm1Hela homozygotes
• 2 to 4 days following tamoxifen treatment
• 2 to 4 days following tamoxifen treatment the proximal intestine is devoid of food suggesting intestinal blockage

growth/size/body
• following tamoxifen treatment

cellular
• following tamoxifen treatment, goblet cells are lost unlike in Elavl1tm1Hela homozygotes
• following tamoxifen treatment, early B cells exhibit increased apoptosis and necrosis and decreased proliferation compared with B cells from Elavl1tm1Hela homozygotes
• following tamoxifen treatment, double positive T cells in the thymus exhibit increased apoptosis and necrosis and decreased proliferation compared with T cells from Elavl1tm1Hela homozygotes
• mouse embryonic fibroblasts treated with 4-hydoxytamoxifen exhibit decreased proliferation compared with similarly treated cells from Elavl1tm1Hela homozygotes

endocrine/exocrine glands
• following tamoxifen treatment, proliferation of crypt progenitor cells is decreased while apoptosis is increased unlike in Elavl1tm1Hela homozygotes
• following tamoxifen treatment





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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