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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tnfrsf11btm1Eac
targeted mutation 1, Edward A Clark
MGI:2179712
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Tnfrsf11btm1Eac/Tnfrsf11btm1Eac involves: 129S4/SvJaeSor MGI:3852640
cx2
Apoetm1Unc/Apoetm1Unc
Tnfrsf11btm1Eac/Tnfrsf11btm1Eac
involves: 129S4/SvJaeSor * C57BL/6 MGI:3852641


Genotype
MGI:3852640
hm1
Allelic
Composition
Tnfrsf11btm1Eac/Tnfrsf11btm1Eac
Genetic
Background
involves: 129S4/SvJaeSor
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tnfrsf11btm1Eac mutation (1 available); any Tnfrsf11b mutation (29 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
skeleton
• thickened mandibular corpus
• fractured diaphyses of long bones often seen in older mice
• shortened femoral neck in 2 month old mice
• increased outer diameter of long bones
• dramatically reduced bone density in 3 month old males
• cortical bone is more porous

immune system
• defective pro-B cell to pre-B cell transition
• increased proliferative response to IL-7 (1.7-2 fold increase)
• increased number of peripheral B cells
• 53% more IgM (high) IgD (low) B cells
• variable ability to mount an antibody response
• antibody response is comparable to controls overall
• enhanced ability to stimulate T-cell proliferation

limbs/digits/tail
• shortened femoral neck in 2 month old mice

craniofacial
• thickened mandibular corpus

hematopoietic system
• defective pro-B cell to pre-B cell transition
• increased proliferative response to IL-7 (1.7-2 fold increase)
• increased number of peripheral B cells
• 53% more IgM (high) IgD (low) B cells
• variable ability to mount an antibody response
• antibody response is comparable to controls overall




Genotype
MGI:3852641
cx2
Allelic
Composition
Apoetm1Unc/Apoetm1Unc
Tnfrsf11btm1Eac/Tnfrsf11btm1Eac
Genetic
Background
involves: 129S4/SvJaeSor * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Apoetm1Unc mutation (33 available); any Apoe mutation (145 available)
Tnfrsf11btm1Eac mutation (1 available); any Tnfrsf11b mutation (29 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• increased extractable calcium in the aorta at 40 and 60 weeks
• 38% show calcification of the medial layer of the brachiocephalic artery
• calcification of the intimal layer of the brachiocephalic artery by 40-60 weeks
• increased area of lesions in the brachiocephalic artery at 40 and 60 weeks but not at 20 weeks
• increased number of lesions with laminated elastic fibers
• larger areas of collagen and proteoglycan deposition
• 40% addition reduction in lesion cellularity as compared to mice only homozygous for Apoetm1Unc





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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory