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When bred to different strains expressing Cre recombinase in various tissues, this strain may be useful in studies such as chrondocyte differentiation, cardiovascular disease, brain malformation and studies of craniofacial, lung, bone and tooth development.


Strain Information

Former Names B6.129-Ctnnb1tm2Kem/J    (Changed: 29-NOV-05 )
B6.129-Catnbtm2Kem/J    (Changed: 20-MAY-05 )
Type Congenic; Targeted Mutation;
Additional information on Genetically Engineered and Mutant Mice.
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Additional information on Congenic nomenclature.
Mating SystemHomozygote x Homozygote         (Female x Male)   01-MAR-06
Specieslaboratory mouse
GenerationN10F?+F12N2F5 (22-JAN-15)
Generation Definitions
Donating InvestigatorProf. Dr. RolfK Kemler,   Max Planck Institute for Immunobiology

These mice possess loxP sites located in introns 1 and 6 of the targeted gene. Mice that are homozygous for this floxed allele are viable, fertile, normal in size and do not display any gross physical or behavioral abnormalities.

When bred to a strain expressing Cre recombinase in chrondocytes (see Stock No. 003554 for example), this mutant mouse strain may be useful in studies of chrondocyte differentiation.

When bred to a strain expressing Cre recombinase in heart(see Stock No. 005650 or 005657 for example), this mutant mouse strain may be useful in studies of cardiovascular disease.

When bred to a strain expressing Cre recombinase in midbrain/dorsal spinal cord (see Stock No. 007807 or 009107 for example), this mutant mouse strain may be useful in studies of brain malformation and craniofacial development.

When bred to a strain expressing Cre recombinase in the distal posterior region of the embryo (see Stock No. 005622 for example), this mutant mouse strain may be useful in studies of lung development.

When bred to a strain expressing Cre recombinase in palate (see Stock No. 009388 for example), this mutant mouse strain may be useful in studies of tooth development.

When bred to a strain expressing Cre recombinase in early limb bud mesenchyme and a subset of craniofacial mesenchyme (see Stock No. 005584 for example), this mutant mouse strain may be useful in studies of bone development.

When bred to mice carrying Tg(Krt1-15-cre/PGR)22Cot (Stock No. 005249), RU 486-induced Cre recombinase expression in the epithelial and hair follicle results in altered hair growth.

When bred to mice carrying Tg(KRT14-cre/ERT)20Efu (Stock No. 005107), tamoxifen-inducible Cre recombinase expression in the epidermis results in increased cell proliferation and increased numbers of mast cells.

A targeting vector containing neomycin resistance and herpes simplex virus thymidine kinase genes was utilized in the construction of this mutant. Similarly oriented loxP sites were placed upstream of exon 2 and flanking the neomycin resistance/ thymidine kinase genes (located in intron 6). The construct was electroporated into 129X1/SvJ x 129S1/Sv-derived R1 embryonic stem (ES) cells. Correctly targeted ES cells were transiently transfected with a Cre expression plasmid for the purpose of removing the selectable marker cassette. ES cells that had successfully undergone Cre recombination and no longer retained the cassette but did retain the loxP-flanked exons 2-6 were injected in C57BL/6J blastocysts. Resulting chimeric male animals were backcrossed to wild-type C57BL/6J mice.

Control Information

   000664 C57BL/6J
  Considerations for Choosing Controls

Additional Web Information

Introduction to Cre-lox technology


Phenotype Information

View Related Disease (OMIM) Terms

Related Disease (OMIM) Terms provided by MGI
- Potential model based on gene homology relationships. Phenotypic similarity to the human disease has not been tested.
Colorectal Cancer; CRC   (CTNNB1)
Hepatocellular Carcinoma   (CTNNB1)
Mental Retardation, Autosomal Dominant 19; MRD19   (CTNNB1)
Ovarian Cancer   (CTNNB1)
Pilomatrixoma   (CTNNB1)
View Mammalian Phenotype Terms

Mammalian Phenotype Terms provided by MGI
      assigned by genotype

The following phenotype information is associated with a similar, but not exact match to this JAX® Mice strain.


        involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * FVB/N   (conditional)
  • cardiovascular system phenotype
  • decreased response of heart to induced stress
    • mutants treated with tamoxifen and subjected to thoracic aortic constriction exhibit a reduced hypertrophic response to the pressure overload   (MGI Ref ID J:109612)
  • homeostasis/metabolism phenotype
  • decreased response of heart to induced stress
    • mutants treated with tamoxifen and subjected to thoracic aortic constriction exhibit a reduced hypertrophic response to the pressure overload   (MGI Ref ID J:109612)

The following phenotype relates to a compound genotype created using this strain.
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Ctnnb1tm2Kem/Ctnnb1+ Lyz2tm1(cre)Ifo/Lyz2+

        involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ   (conditional)
  • skeleton phenotype
  • decreased trabecular bone volume   (MGI Ref ID J:178340)
  • increased bone resorption   (MGI Ref ID J:178340)
  • increased osteoclast cell number   (MGI Ref ID J:178340)
  • osteoporosis   (MGI Ref ID J:178340)
  • hematopoietic system phenotype
  • increased osteoclast cell number   (MGI Ref ID J:178340)
  • immune system phenotype
  • increased osteoclast cell number   (MGI Ref ID J:178340)

Ctnnb1tm2Kem/Ctnnb1+ Tg(Prrx1-cre)1Cjt/0

        involves: 129 * C57BL/6 * SJL   (conditional)
  • skeleton phenotype
  • abnormal skeleton morphology
    • slight reduction in bone size   (MGI Ref ID J:173242)

Ctnnb1tm2Kem/Ctnnb1+ Tg(Tek-cre)1Ywa/0

        involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL   (conditional)
  • skeleton phenotype
  • decreased trabecular bone volume   (MGI Ref ID J:178340)
  • increased bone resorption   (MGI Ref ID J:178340)
  • increased osteoclast cell number   (MGI Ref ID J:178340)
  • osteoporosis   (MGI Ref ID J:178340)
  • hematopoietic system phenotype
  • increased osteoclast cell number   (MGI Ref ID J:178340)
  • immune system phenotype
  • increased osteoclast cell number   (MGI Ref ID J:178340)

Ctnnb1tm2Kem/Ctnnb1tm2.1Kem Tg(Sox2-cre)1Amc/0

        involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6 * CBA   (conditional)
  • mortality/aging
  • complete prenatal lethality   (MGI Ref ID J:187739)
  • embryogenesis phenotype
  • abnormal embryonic tissue morphology
    • absence of embryonic structures at E8.5   (MGI Ref ID J:187739)

Ctnnb1tm2Kem/Ctnnb1tm2.1Kem Tg(Wnt1-cre)11Rth/?

        involves: 129/Sv * C57BL/6 * CBA   (conditional)
  • mortality/aging
  • complete prenatal lethality
    • no mutant mice are born   (MGI Ref ID J:67966)
  • craniofacial phenotype
  • absent craniofacial bones
    • craniofacial bones derived from neural crest cells are absent   (MGI Ref ID J:67966)
    • bones present include optic vesicle, basioccipital, exoccipital   (MGI Ref ID J:67966)
  • skeleton phenotype
  • absent craniofacial bones
    • craniofacial bones derived from neural crest cells are absent   (MGI Ref ID J:67966)
    • bones present include optic vesicle, basioccipital, exoccipital   (MGI Ref ID J:67966)
  • nervous system phenotype
  • abnormal brain morphology   (MGI Ref ID J:67966)
    • abnormal brain development
      • brain morphogenesis grossly abnormal between E10.5 and 18.5   (MGI Ref ID J:67966)
      • absent midbrain-hindbrain boundary
        • isthmic border between midbrain and rhombencephalon not visible   (MGI Ref ID J:67966)
    • abnormal hindbrain morphology
      • anterior hindbrain is missing by E10.5   (MGI Ref ID J:67966)
      • poorly formed connections between cranial ganglia and hindbrain   (MGI Ref ID J:67966)
      • absent cerebellum
        • cerebellum is missing at E12.5   (MGI Ref ID J:67966)
      • absent metencephalon
        • anterior hindbrain is missing by E10.5   (MGI Ref ID J:67966)
    • abnormal telencephalon morphology
      • enlarged telencephalon   (MGI Ref ID J:67966)
      • walls of cephalic vesicles thinner   (MGI Ref ID J:67966)
    • abnormal trigeminal V mesencephalic nucleus morphology
      • indistinctly formed   (MGI Ref ID J:67966)
    • absent choroid plexus
      • choroid plexus absent by E12.5   (MGI Ref ID J:67966)
    • absent midbrain
      • by E10.5 parts of the midbrain are missing   (MGI Ref ID J:67966)
      • no discernable midbrain by E12.5   (MGI Ref ID J:67966)
  • abnormal cranial nerve morphology   (MGI Ref ID J:67966)
    • abnormal facial nerve morphology
      • combined ganglion with vestibulocochlear nerve abnormal   (MGI Ref ID J:67966)
    • abnormal glossopharyngeal nerve morphology
      • roots poorly formed   (MGI Ref ID J:67966)
    • abnormal hypoglossal nerve morphology
      • roots poorly formed   (MGI Ref ID J:67966)
      • hypoglossal nerve missing   (MGI Ref ID J:67966)
    • abnormal vagus nerve morphology
      • roots poorly formed   (MGI Ref ID J:67966)
    • absent oculomotor nerve   (MGI Ref ID J:67966)
  • abnormal dorsal root ganglion morphology
    • first spinal root ganglion missing   (MGI Ref ID J:67966)
    • other spinal root ganglia severely affected as well   (MGI Ref ID J:67966)
  • abnormal neural tube morphology/development
    • shortened neural tube   (MGI Ref ID J:67966)
  • embryogenesis phenotype
  • abnormal neural tube morphology/development
    • shortened neural tube   (MGI Ref ID J:67966)

Ctnnb1tm2Kem/Ctnnb1tm2.1Kem Tg(Zp3-cre)93Knw/0

        involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6J   (conditional)
  • mortality/aging
  • complete prenatal lethality   (MGI Ref ID J:187739)
  • embryogenesis phenotype
  • abnormal embryonic tissue morphology
    • absence of embryonic structures at E8.5   (MGI Ref ID J:187739)

Ctnnb1tm2Kem/Ctnnb1tm2Kem Gt(ROSA)26Sortm1Sor/Gt(ROSA)26Sor+ Tg(Wnt1-cre)11Rth/0

        involves: 129 * C57BL/6 * CBA/J   (conditional)
  • craniofacial phenotype
  • absent mandible
  • absent maxilla
  • small pharyngeal arch
    • rudimentary at E12.5   (MGI Ref ID J:178971)
  • nervous system phenotype
  • absent hindbrain
    • absence of hindbrain structures at E10.5   (MGI Ref ID J:178971)
  • absent midbrain-hindbrain boundary
    • absent at E10.5   (MGI Ref ID J:178971)
  • absent midbrain
    • absence of midbrain structures at E10.5   (MGI Ref ID J:178971)
  • embryogenesis phenotype
  • small pharyngeal arch
    • rudimentary at E12.5   (MGI Ref ID J:178971)
  • skeleton phenotype
  • absent mandible
  • absent maxilla

Ctnnb1tm2Kem/Ctnnb1tm2Kem Lyz2tm1(cre)Ifo/Lyz2+

        involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ   (conditional)
  • skeleton phenotype
  • decreased trabecular bone volume   (MGI Ref ID J:178340)
  • increased bone resorption   (MGI Ref ID J:178340)
  • increased osteoclast cell number   (MGI Ref ID J:178340)
  • osteoporosis   (MGI Ref ID J:178340)
  • hematopoietic system phenotype
  • increased osteoclast cell number   (MGI Ref ID J:178340)
  • immune system phenotype
  • increased osteoclast cell number   (MGI Ref ID J:178340)

Ctnnb1tm2Kem/Ctnnb1tm2Kem Shhtm1(EGFP/cre)Cjt/Shh+

        involves: 129S1/Sv * 129X1/SvJ   (conditional)
  • respiratory system phenotype
  • abnormal lung development
    • mice exhibit an expansion of lung endoderm progenitor cells into the stomach unlike in wild-type mice   (MGI Ref ID J:153098)
    • absent lung buds
      • mice lack tracheal budding   (MGI Ref ID J:153098)
  • absent lungs
    • mice lack lung specification   (MGI Ref ID J:153098)

Ctnnb1tm2Kem/Ctnnb1tm2Kem Tg(Col2a1-cre)1Bhr/0

        involves: 129S1/Sv * 129X1/SvJ   (conditional)
  • craniofacial phenotype
  • abnormal craniofacial bone morphology   (MGI Ref ID J:90567)
    • domed cranium   (MGI Ref ID J:90567)
  • limbs/digits/tail phenotype
  • short limbs   (MGI Ref ID J:90567)
  • skeleton phenotype
  • abnormal cartilage morphology   (MGI Ref ID J:90567)
    • abnormal chondrocyte morphology
      • chondrocyte morphology reduced about 34%   (MGI Ref ID J:90567)
  • abnormal craniofacial bone morphology   (MGI Ref ID J:90567)
    • domed cranium   (MGI Ref ID J:90567)
  • decreased length of long bones
    • endochondral bone elements all shorter   (MGI Ref ID J:90567)

Ctnnb1tm2Kem/Ctnnb1tm2Kem Tg(KRT14-cre/ERT)20Efu/0

        involves: 129S1/Sv * 129X1/SvJ * CD-1   (conditional)
  • integument phenotype
  • *normal* integument phenotype
    • after induction, mutants do not display overt blistering   (MGI Ref ID J:204142)
    • abnormal epidermal layer morphology
      • with topical tamoxifen treatment during the first telogen phase, epidermis exhibits increased proliferation as well as expanded expression of basal and suprabasal markers and hyperproliferation markers   (MGI Ref ID J:204142)
  • immune system phenotype
  • increased mast cell number
    • with doxycycline induction from P4-P60, mast cell number in the dermis is increased at P60   (MGI Ref ID J:204142)
  • hematopoietic system phenotype
  • increased mast cell number
    • with doxycycline induction from P4-P60, mast cell number in the dermis is increased at P60   (MGI Ref ID J:204142)

Ctnnb1tm2Kem/Ctnnb1tm2Kem Tg(Krt1-15-cre/PGR)22Cot/0

        involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL   (conditional)
  • integument phenotype
  • *normal* integument phenotype
    • when induction is performed from P20-27, upper hair follicles and sebaceous glands are intact   (MGI Ref ID J:204142)
    • hyperproliferation is not observed in the epidermis   (MGI Ref ID J:204142)
    • abnormal hair cycle anagen phase
      • when animals are treated topically with RU486 for 5 days prior to hair plucking at P54, hair follicles in treated areas do not progress through anagen, while controls show robust hair regrowth 14 days after plucking   (MGI Ref ID J:204142)
    • abnormal hair follicle morphology
      • when induction is performed from P20-27, secondary hair germ cells in some mutant hair follicles appear abnormal or absent at P60   (MGI Ref ID J:204142)
    • abnormal hair growth
      • after treatment of skin with RU486 to induce cre deletion, external hair growth fails   (MGI Ref ID J:204142)

Ctnnb1tm2Kem/Ctnnb1tm2Kem Tg(Tek-cre)1Ywa/0

        involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL   (conditional)
  • mortality/aging
  • partial prenatal lethality
    • fewer than expected mice are born   (MGI Ref ID J:178340)
  • skeleton phenotype
  • decreased bone resorption   (MGI Ref ID J:178340)
  • decreased osteoclast cell number   (MGI Ref ID J:178340)
  • increased bone volume   (MGI Ref ID J:178340)
  • osteopetrosis   (MGI Ref ID J:178340)
  • hematopoietic system phenotype
  • decreased osteoclast cell number   (MGI Ref ID J:178340)
  • immune system phenotype
  • decreased osteoclast cell number   (MGI Ref ID J:178340)

Ctnnb1tm2Kem/Ctnnb1tm2Kem Tg(Wnt1-cre)11Rth/0

        involves: 129 * C57BL/6 * CBA/J   (conditional)
  • nervous system phenotype
  • abnormal neural tube morphology/development
    • disruption of apical neural tube morphology leading to migration of cells into the neural canal   (MGI Ref ID J:178971)
  • abnormal telencephalon development
    • malformed telencephalic lobes at E12.5   (MGI Ref ID J:178971)
  • absent midbrain-hindbrain boundary
    • absent at E12.5   (MGI Ref ID J:178971)
  • premature neuronal precursor differentiation   (MGI Ref ID J:178971)
  • craniofacial phenotype
  • abnormal craniofacial morphology
  • embryogenesis phenotype
  • abnormal neural tube morphology/development
    • disruption of apical neural tube morphology leading to migration of cells into the neural canal   (MGI Ref ID J:178971)
  • cellular phenotype
  • premature neuronal precursor differentiation   (MGI Ref ID J:178971)

Ctnnb1tm2Kem/Ctnnb1+ Osr2tm2(cre)Jian/Osr2+

        involves: 129S1/Sv * 129X1/SvJ   (conditional)
  • mortality/aging
  • neonatal lethality   (MGI Ref ID J:153554)
  • craniofacial phenotype
  • abnormal tooth development
    • unlike in wild-type mice, strong Caspase3 activity is detected in the enamel knot cells of the maxillary and mandibular first molar tooth germs at E14.5   (MGI Ref ID J:153554)
    • however, no increase in cell death in tooth epithelium and mesenchyme is detected   (MGI Ref ID J:153554)
    • growth retardation of incisors
      • incisor development arrests at bud stage   (MGI Ref ID J:153554)
    • growth retardation of molars
      • molar development arrests at bud stage   (MGI Ref ID J:153554)
  • cleft secondary palate   (MGI Ref ID J:153554)
  • digestive/alimentary phenotype
  • cleft secondary palate   (MGI Ref ID J:153554)
  • growth/size/body region phenotype
  • abnormal tooth development
    • unlike in wild-type mice, strong Caspase3 activity is detected in the enamel knot cells of the maxillary and mandibular first molar tooth germs at E14.5   (MGI Ref ID J:153554)
    • however, no increase in cell death in tooth epithelium and mesenchyme is detected   (MGI Ref ID J:153554)
    • growth retardation of incisors
      • incisor development arrests at bud stage   (MGI Ref ID J:153554)
    • growth retardation of molars
      • molar development arrests at bud stage   (MGI Ref ID J:153554)
  • cleft secondary palate   (MGI Ref ID J:153554)

Ctnnb1tm2Kem/Ctnnb1tm2Kem Osr2tm2(cre)Jian/Osr2+

        involves: 129S1/Sv * 129X1/SvJ   (conditional)
  • skeleton phenotype
  • abnormal joint morphology
    • at E13.5, joints are not as clearly organized as in wild-type mice   (MGI Ref ID J:171478)
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Research Applications
This mouse can be used to support research in many areas including:

Research Tools
Cre-lox System
      loxP-flanked Sequences
Developmental Biology Research
      Cre-lox System

Ctnnb1tm2Kem related

Developmental Biology Research
Defects in Cell Adhesion Molecules

Genes & Alleles

Gene & Allele Information provided by MGI

Allele Symbol Ctnnb1tm2Kem
Allele Name targeted mutation 2, Rolf Kemler
Allele Type Targeted (Conditional ready (e.g. floxed), No functional change)
Common Name(s) B-cateninfl2-6; BcatLOF; Beta-Catc; Catnb1tm2Kem; Catnbfx; Catnblox(ex2-6); Catnbtm2Kem; Catnbtm2Kwem; CtnbfloxE2-E6; Ctnnb1f; Ctnnb1flox; Ctnnb1floxed; Ctnnb1fx; Ctnnb1loxp; beta-Catflox; beta-Ctnfl; beta-catex2-6; beta-catfl; beta-catlof; beta-catenin/loxP(ex2-6); beta-cateninc; beta-cateninf; beta-cateninfl; beta-cateninflox; beta-cateninfloxed; beta-cateninlox;
Mutation Made ByProf. Dr. RolfK Kemler,   Max Planck Institute for Immunobiology
Strain of Origin(129X1/SvJ x 129S1/Sv)F1-Kitl<+>
ES Cell Line NameR1
ES Cell Line Strain(129X1/SvJ x 129S1/Sv)F1-Kitl<+>
Gene Symbol and Name Ctnnb1, catenin (cadherin associated protein), beta 1
Chromosome 9
Gene Common Name(s) Bfc; CTNNB; Catnb; MRD19; armadillo; batface; beta catenin; beta-catenin; catenin beta;
Molecular Note A loxP site was inserted in intron 1 and a loxP-flanked neomycin-TK cassette was inserted downstream in intron 6. The neomycin-TK cassette was removed by transient transfection with a Cre recombinase expression vector in ES cells prior to the production of chimeric mice and left two loxP sites flanking a region of gene sequence from exon 2 through exon 6. [MGI Ref ID J:67966]


Genotyping Information

Genotyping Protocols

Ctnnb1tm2Kem, Standard PCR

Helpful Links

Genotyping resources and troubleshooting


References provided by MGI

Selected Reference(s)

Brault V; Moore R; Kutsch S; Ishibashi M; Rowitch DH; McMahon AP; Sommer L; Boussadia O; Kemler R. 2001. Inactivation of the beta-catenin gene by Wnt1-Cre-mediated deletion results in dramatic brain malformation and failure of craniofacial development. Development 128(8):1253-64. [PubMed: 11262227]  [MGI Ref ID J:67966]

Additional References

Akiyama H; Lyons JP; Mori-Akiyama Y; Yang X; Zhang R; Zhang Z; Deng JM; Taketo MM; Nakamura T; Behringer RR; McCrea PD; de Crombrugghe B. 2004. Interactions between Sox9 and beta-catenin control chondrocyte differentiation. Genes Dev 18(9):1072-87. [PubMed: 15132997]  [MGI Ref ID J:90567]

Campos VE; Du M; Li Y. 2004. Increased seizure susceptibility and cortical malformation in beta-catenin mutant mice. Biochem Biophys Res Commun 320(2):606-14. [PubMed: 15219872]  [MGI Ref ID J:92923]

Ctnnb1tm2Kem related

Ahn Y; Sims C; Logue JM; Weatherbee SD; Krumlauf R. 2013. Lrp4 and Wise interplay controls the formation and patterning of mammary and other skin appendage placodes by modulating Wnt signaling. Development 140(3):583-93. [PubMed: 23293290]  [MGI Ref ID J:194074]

Ahrens MJ; Li Y; Jiang H; Dudley AT. 2009. Convergent extension movements in growth plate chondrocytes require gpi-anchored cell surface proteins. Development 136(20):3463-74. [PubMed: 19762422]  [MGI Ref ID J:153618]

Ahrens MJ; Romereim S; Dudley AT. 2011. A re-evaluation of two key reagents for in vivo studies of Wnt signaling. Dev Dyn :. [PubMed: 21793100]  [MGI Ref ID J:174609]

Ai D; Fu X; Wang J; Lu MF; Chen L; Baldini A; Klein WH; Martin JF. 2007. Canonical Wnt signaling functions in second heart field to promote right ventricular growth. Proc Natl Acad Sci U S A 104(22):9319-24. [PubMed: 17519332]  [MGI Ref ID J:143626]

Akiyama H; Lyons JP; Mori-Akiyama Y; Yang X; Zhang R; Zhang Z; Deng JM; Taketo MM; Nakamura T; Behringer RR; McCrea PD; de Crombrugghe B. 2004. Interactions between Sox9 and beta-catenin control chondrocyte differentiation. Genes Dev 18(9):1072-87. [PubMed: 15132997]  [MGI Ref ID J:90567]

Akiyama R; Kawakami H; Taketo MM; Evans SM; Wada N; Petryk A; Kawakami Y. 2014. Distinct populations within Isl1 lineages contribute to appendicular and facial skeletogenesis through the beta-catenin pathway. Dev Biol 387(1):37-48. [PubMed: 24424161]  [MGI Ref ID J:207610]

Albers J; Keller J; Baranowsky A; Beil FT; Catala-Lehnen P; Schulze J; Amling M; Schinke T. 2013. Canonical Wnt signaling inhibits osteoclastogenesis independent of osteoprotegerin. J Cell Biol 200(4):537-49. [PubMed: 23401003]  [MGI Ref ID J:195205]

Amini-Nik S; Cambridge E; Yu W; Guo A; Whetstone H; Nadesan P; Poon R; Hinz B; Alman BA. 2014. beta-Catenin-regulated myeloid cell adhesion and migration determine wound healing. J Clin Invest 124(6):2599-610. [PubMed: 24837430]  [MGI Ref ID J:212902]

Anderson MJ; Naiche LA; Wilson CP; Elder C; Swing DA; Lewandoski M. 2013. TCreERT2, a transgenic mouse line for temporal control of Cre-mediated recombination in lineages emerging from the primitive streak or tail bud. PLoS One 8(4):e62479. [PubMed: 23638095]  [MGI Ref ID J:200549]

Andoniadou CL; Signore M; Young RM; Gaston-Massuet C; Wilson SW; Fuchs E; Martinez-Barbera JP. 2011. HESX1- and TCF3-mediated repression of Wnt/beta-catenin targets is required for normal development of the anterior forebrain. Development 138(22):4931-42. [PubMed: 22007134]  [MGI Ref ID J:181005]

Apte U; Singh S; Zeng G; Cieply B; Virji MA; Wu T; Monga SP. 2009. Beta-catenin activation promotes liver regeneration after acetaminophen-induced injury. Am J Pathol 175(3):1056-65. [PubMed: 19679878]  [MGI Ref ID J:152895]

Apte U; Zeng G; Muller P; Tan X; Micsenyi A; Cieply B; Dai C; Liu Y; Kaestner KH; Monga SP. 2006. Activation of Wnt/beta-catenin pathway during hepatocyte growth factor-induced hepatomegaly in mice. Hepatology 44(4):992-1002. [PubMed: 17006939]  [MGI Ref ID J:115725]

Apte U; Zeng G; Thompson MD; Muller P; Micsenyi A; Cieply B; Kaestner KH; Monga SP. 2007. beta-Catenin is critical for early postnatal liver growth. Am J Physiol Gastrointest Liver Physiol 292(6):G1578-85. [PubMed: 17332475]  [MGI Ref ID J:123695]

Arango NA; Szotek PP; Manganaro TF; Oliva E; Donahoe PK; Teixeira J. 2005. Conditional deletion of beta-catenin in the mesenchyme of the developing mouse uterus results in a switch to adipogenesis in the myometrium. Dev Biol 288(1):276-83. [PubMed: 16256976]  [MGI Ref ID J:103530]

Armstrong A; Ryu YK; Chieco D; Kuruvilla R. 2011. Frizzled3 Is Required for Neurogenesis and Target Innervation during Sympathetic Nervous System Development. J Neurosci 31(7):2371-81. [PubMed: 21325504]  [MGI Ref ID J:169444]

Aulehla A; Wiegraebe W; Baubet V; Wahl MB; Deng C; Taketo M; Lewandoski M; Pourquie O. 2008. A beta-catenin gradient links the clock and wavefront systems in mouse embryo segmentation. Nat Cell Biol 10(2):186-93. [PubMed: 18157121]  [MGI Ref ID J:132361]

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Sarin S; Boivin F; Li A; Lim J; Svajger B; Rosenblum ND; Bridgewater D. 2014. beta-Catenin Overexpression in the Metanephric Mesenchyme Leads to Renal Dysplasia Genesis via Cell-Autonomous and Non-Cell-Autonomous Mechanisms. Am J Pathol 184(5):1395-410. [PubMed: 24637293]  [MGI Ref ID J:208128]

Schuller U; Rowitch DH. 2007. Beta-catenin function is required for cerebellar morphogenesis. Brain Res 1140:161-9. [PubMed: 16824494]  [MGI Ref ID J:120586]

Sekine S; Gutierrez PJ; Lan BY; Feng S; Hebrok M. 2007. Liver-specific loss of beta-catenin results in delayed hepatocyte proliferation after partial hepatectomy. Hepatology 45(2):361-8. [PubMed: 17256747]  [MGI Ref ID J:153936]

Sekine S; Lan BY; Bedolli M; Feng S; Hebrok M. 2006. Liver-specific loss of beta-catenin blocks glutamine synthesis pathway activity and cytochrome p450 expression in mice. Hepatology 43(4):817-25. [PubMed: 16557553]  [MGI Ref ID J:153937]

Sekine S; Ogawa R; Kanai Y. 2011. Hepatomas with activating Ctnnb1 mutations in 'Ctnnb1-deficient' livers: a tricky aspect of a conditional knockout mouse model. Carcinogenesis 32(4):622-8. [PubMed: 21216847]  [MGI Ref ID J:170659]

Sekine S; Ogawa R; Mcmanus MT; Kanai Y; Hebrok M. 2009. Dicer is required for proper liver zonation. J Pathol 219(3):365-72. [PubMed: 19718708]  [MGI Ref ID J:153733]

Shan M; Gentile M; Yeiser JR; Walland AC; Bornstein VU; Chen K; He B; Cassis L; Bigas A; Cols M; Comerma L; Huang B; Blander JM; Xiong H; Mayer L; Berin C; Augenlicht LH; Velcich A; Cerutti A. 2013. Mucus enhances gut homeostasis and oral tolerance by delivering immunoregulatory signals. Science 342(6157):447-53. [PubMed: 24072822]  [MGI Ref ID J:202829]

Shi F; Hu L; Jacques BE; Mulvaney JF; Dabdoub A; Edge AS. 2014. beta-Catenin is required for hair-cell differentiation in the cochlea. J Neurosci 34(19):6470-9. [PubMed: 24806673]  [MGI Ref ID J:211047]

Simons BW; Hurley PJ; Huang Z; Ross AE; Miller R; Marchionni L; Berman DM; Schaeffer EM. 2012. Wnt signaling though beta-catenin is required for prostate lineage specification. Dev Biol 371(2):246-55. [PubMed: 22960283]  [MGI Ref ID J:190538]

Smith AN; Miller LA; Song N; Taketo MM; Lang RA. 2005. The duality of beta-catenin function: a requirement in lens morphogenesis and signaling suppression of lens fate in periocular ectoderm. Dev Biol 285(2):477-89. [PubMed: 16102745]  [MGI Ref ID J:101264]

Smith MK; Koch PJ; Reynolds SD. 2012. Direct and indirect roles for beta-catenin in facultative basal progenitor cell differentiation. Am J Physiol Lung Cell Mol Physiol 302(6):L580-94. [PubMed: 22227204]  [MGI Ref ID J:183435]

Song N; Schwab KR; Patterson LT; Yamaguchi T; Lin X; Potter SS; Lang RA. 2007. pygopus 2 has a crucial, Wnt pathway-independent function in lens induction. Development 134(10):1873-85. [PubMed: 17428831]  [MGI Ref ID J:121416]

Spittau B; Wullkopf L; Zhou X; Rilka J; Pfeifer D; Krieglstein K. 2013. Endogenous transforming growth factor-beta promotes quiescence of primary microglia in vitro. Glia 61(2):287-300. [PubMed: 23065670]  [MGI Ref ID J:191135]

Stenman JM; Rajagopal J; Carroll TJ; Ishibashi M; McMahon J; McMahon AP. 2008. Canonical Wnt signaling regulates organ-specific assembly and differentiation of CNS vasculature. Science 322(5905):1247-50. [PubMed: 19023080]  [MGI Ref ID J:142352]

Sun X; Jackson L; Dey SK; Daikoku T. 2009. In pursuit of leucine-rich repeat-containing G protein-coupled receptor-5 regulation and function in the uterus. Endocrinology 150(11):5065-73. [PubMed: 19797400]  [MGI Ref ID J:157315]

Sun Y; Aiga M; Yoshida E; Humbert PO; Bamji SX. 2009. Scribble interacts with beta-catenin to localize synaptic vesicles to synapses. Mol Biol Cell 20(14):3390-400. [PubMed: 19458197]  [MGI Ref ID J:153473]

Sun Y; Teng I; Huo R; Rosenfeld MG; Olson LE; Li X; Li X. 2012. Asymmetric requirement of surface epithelial beta-catenin during the upper and lower jaw development. Dev Dyn 241(4):663-74. [PubMed: 22354888]  [MGI Ref ID J:181632]

Swope D; Cheng L; Gao E; Li J; Radice GL. 2012. Loss of cadherin-binding proteins beta-catenin and plakoglobin in the heart leads to gap junction remodeling and arrhythmogenesis. Mol Cell Biol 32(6):1056-67. [PubMed: 22252313]  [MGI Ref ID J:183710]

Takezawa Y; Yoshida K; Miyado K; Sato M; Nakamura A; Kawano N; Sakakibara K; Kondo T; Harada Y; Ohnami N; Kanai S; Miyado M; Saito H; Takahashi Y; Akutsu H; Umezawa A. 2011. beta-catenin is a molecular switch that regulates transition of cell-cell adhesion to fusion. Sci Rep 1:68. [PubMed: 22355587]  [MGI Ref ID J:206123]

Tamarina NA; Roe MW; Philipson L. 2014. Characterization of mice expressing Ins1 gene promoter driven CreERT recombinase for conditional gene deletion in pancreatic beta-cells. Islets 6(1):. [PubMed: 24637233]  [MGI Ref ID J:208033]

Tan X; Behari J; Cieply B; Michalopoulos GK; Monga SP. 2006. Conditional deletion of beta-catenin reveals its role in liver growth and regeneration. Gastroenterology 131(5):1561-72. [PubMed: 17101329]  [MGI Ref ID J:124952]

Tang M; Miyamoto Y; Huang EJ. 2009. Multiple roles of {beta}-catenin in controlling the neurogenic niche for midbrain dopamine neurons. Development 136(12):2027-38. [PubMed: 19439492]  [MGI Ref ID J:149534]

Taniguchi N; Carames B; Kawakami Y; Amendt BA; Komiya S; Lotz M. 2009. Chromatin protein HMGB2 regulates articular cartilage surface maintenance via beta-catenin pathway. Proc Natl Acad Sci U S A 106(39):16817-22. [PubMed: 19805379]  [MGI Ref ID J:153213]

Tao GZ; Lehwald N; Jang KY; Baek J; Xu B; Omary MB; Sylvester KG. 2013. Wnt/beta-catenin signaling protects mouse liver against oxidative stress-induced apoptosis through the inhibition of forkhead transcription factor FoxO3. J Biol Chem 288(24):17214-24. [PubMed: 23620592]  [MGI Ref ID J:199603]

Tian Y; Yuan L; Goss AM; Wang T; Yang J; Lepore JJ; Zhou D; Schwartz RJ; Patel V; Cohen ED; Morrisey EE. 2010. Characterization and in vivo pharmacological rescue of a Wnt2-Gata6 pathway required for cardiac inflow tract development. Dev Cell 18(2):275-87. [PubMed: 20159597]  [MGI Ref ID J:158582]

Tran TH; Jarrell A; Zentner GE; Welsh A; Brownell I; Scacheri PC; Atit R. 2010. Role of canonical Wnt signaling/ss-catenin via Dermo1 in cranial dermal cell development. Development 137(23):3973-84. [PubMed: 20980404]  [MGI Ref ID J:166907]

Tsai SY; Sennett R; Rezza A; Clavel C; Grisanti L; Zemla R; Najam S; Rendl M. 2014. Wnt/beta-catenin signaling in dermal condensates is required for hair follicle formation. Dev Biol 385(2):179-88. [PubMed: 24309208]  [MGI Ref ID J:205498]

Ueberham E; Glockner P; Gohler C; Straub BK; Teupser D; Schonig K; Braeuning A; Hohn AK; Jerchow B; Birchmeier W; Gaunitz F; Arendt T; Sansom O; Gebhardt R; Ueberham U. 2015. Global increase of p16INK4a in APC-deficient mouse liver drives clonal growth of p16INK4a-negative tumors. Mol Cancer Res 13(2):239-49. [PubMed: 25270420]  [MGI Ref ID J:219679]

Ukita K; Hirahara S; Oshima N; Imuta Y; Yoshimoto A; Jang CW; Oginuma M; Saga Y; Behringer RR; Kondoh H; Sasaki H. 2009. Wnt signaling maintains the notochord fate for progenitor cells and supports the posterior extension of the notochord. Mech Dev 126(10):791-803. [PubMed: 19720144]  [MGI Ref ID J:153634]

Valenta T; Gay M; Steiner S; Draganova K; Zemke M; Hoffmans R; Cinelli P; Aguet M; Sommer L; Basler K. 2011. Probing transcription-specific outputs of beta-catenin in vivo. Genes Dev 25(24):2631-43. [PubMed: 22190459]  [MGI Ref ID J:178971]

Wang EY; Yeh SH; Tsai TF; Huang HP; Jeng YM; Lin WH; Chen WC; Yeh KH; Chen PJ; Chen DS. 2011. Depletion of beta-catenin from mature hepatocytes of mice promotes expansion of hepatic progenitor cells and tumor development. Proc Natl Acad Sci U S A 108(45):18384-9. [PubMed: 22042854]  [MGI Ref ID J:180230]

Wang HT; Zeng L; Chen Q; Zhang X; Liu JW; Lu TJ; Xiong ZQ; Zheng J; Hu ZL. 2015. beta-Catenin is required for maintaining hippocampal morphology during the perinatal period. Neuroscience 284:273-82. [PubMed: 25290010]  [MGI Ref ID J:221459]

Wang XP; O'Connell DJ; Lund JJ; Saadi I; Kuraguchi M; Turbe-Doan A; Cavallesco R; Kim H; Park PJ; Harada H; Kucherlapati R; Maas RL. 2009. Apc inhibition of Wnt signaling regulates supernumerary tooth formation during embryogenesis and throughout adulthood. Development 136(11):1939-49. [PubMed: 19429790]  [MGI Ref ID J:149542]

Wang Y; Krivtsov AV; Sinha AU; North TE; Goessling W; Feng Z; Zon LI; Armstrong SA. 2010. The Wnt/beta-catenin pathway is required for the development of leukemia stem cells in AML. Science 327(5973):1650-3. [PubMed: 20339075]  [MGI Ref ID J:158885]

Wang Y; Song L; Zhou CJ. 2011. The canonical Wnt/beta-catenin signaling pathway regulates Fgf signaling for early facial development. Dev Biol 349(2):250-60. [PubMed: 21070765]  [MGI Ref ID J:168024]

Weber BN; Chi AW; Chavez A; Yashiro-Ohtani Y; Yang Q; Shestova O; Bhandoola A. 2011. A critical role for TCF-1 in T-lineage specification and differentiation. Nature 476(7358):63-8. [PubMed: 21814277]  [MGI Ref ID J:174921]

Wei W; Wang X; Yang M; Smith LC; Dechow PC; Wan Y. 2010. PGC1beta mediates PPARgamma activation of osteoclastogenesis and rosiglitazone-induced bone loss. Cell Metab 11(6):503-16. [PubMed: 20519122]  [MGI Ref ID J:160910]

Wei W; Zeve D; Suh JM; Wang X; Du Y; Zerwekh JE; Dechow PC; Graff JM; Wan Y. 2011. Biphasic and Dosage-Dependent Regulation of Osteoclastogenesis by beta-Catenin. Mol Cell Biol 31(23):4706-19. [PubMed: 21876000]  [MGI Ref ID J:178340]

Westenskow P; Piccolo S; Fuhrmann S. 2009. Beta-catenin controls differentiation of the retinal pigment epithelium in the mouse optic cup by regulating Mitf and Otx2 expression. Development 136(15):2505-10. [PubMed: 19553286]  [MGI Ref ID J:152855]

Woodhead GJ; Mutch CA; Olson EC; Chenn A. 2006. Cell-autonomous beta-catenin signaling regulates cortical precursor proliferation. J Neurosci 26(48):12620-30. [PubMed: 17135424]  [MGI Ref ID J:116183]

Wray J; Kalkan T; Gomez-Lopez S; Eckardt D; Cook A; Kemler R; Smith A. 2011. Inhibition of glycogen synthase kinase-3 alleviates Tcf3 repression of the pluripotency network and increases embryonic stem cell resistance to differentiation. Nat Cell Biol 13(7):838-45. [PubMed: 21685889]  [MGI Ref ID J:174453]

Wu X; Tu X; Joeng KS; Hilton MJ; Williams DA; Long F. 2008. Rac1 activation controls nuclear localization of beta-catenin during canonical Wnt signaling. Cell 133(2):340-53. [PubMed: 18423204]  [MGI Ref ID J:145305]

Xu B; Chen C; Chen H; Zheng SG; Bringas P Jr; Xu M; Zhou X; Chen D; Umans L; Zwijsen A; Shi W. 2011. Smad1 and its target gene Wif1 coordinate BMP and Wnt signaling activities to regulate fetal lung development. Development 138(5):925-35. [PubMed: 21270055]  [MGI Ref ID J:169137]

Yadav VK; Ryu JH; Suda N; Tanaka KF; Gingrich JA; Schutz G; Glorieux FH; Chiang CY; Zajac JD; Insogna KL; Mann JJ; Hen R; Ducy P; Karsenty G. 2008. Lrp5 controls bone formation by inhibiting serotonin synthesis in the duodenum. Cell 135(5):825-37. [PubMed: 19041748]  [MGI Ref ID J:146078]

Yajima I; Colombo S; Puig I; Champeval D; Kumasaka M; Belloir E; Bonaventure J; Mark M; Yamamoto H; Taketo MM; Choquet P; Etchevers HC; Beermann F; Delmas V; Monassier L; Larue L. 2013. A subpopulation of smooth muscle cells, derived from melanocyte-competent precursors, prevents patent ductus arteriosus. PLoS One 8(1):e53183. [PubMed: 23382837]  [MGI Ref ID J:195917]

Yan Y; Tang D; Chen M; Huang J; Xie R; Jonason JH; Tan X; Hou W; Reynolds D; Hsu W; Harris SE; Puzas JE; Awad H; O'Keefe RJ; Boyce BF; Chen D. 2009. Axin2 controls bone remodeling through the beta-catenin-BMP signaling pathway in adult mice. J Cell Sci 122(Pt 19):3566-78. [PubMed: 19737815]  [MGI Ref ID J:153051]

Yang P; An H; Liu X; Wen M; Zheng Y; Rui Y; Cao X. 2010. The cytosolic nucleic acid sensor LRRFIP1 mediates the production of type I interferon via a beta-catenin-dependent pathway. Nat Immunol 11(6):487-94. [PubMed: 20453844]  [MGI Ref ID J:160697]

Yang Q; Monticelli LA; Saenz SA; Chi AW; Sonnenberg GF; Tang J; De Obaldia ME; Bailis W; Bryson JL; Toscano K; Huang J; Haczku A; Pear WS; Artis D; Bhandoola A. 2013. T cell factor 1 is required for group 2 innate lymphoid cell generation. Immunity 38(4):694-704. [PubMed: 23601684]  [MGI Ref ID J:196648]

Yasuhara R; Ohta Y; Yuasa T; Kondo N; Hoang T; Addya S; Fortina P; Pacifici M; Iwamoto M; Enomoto-Iwamoto M. 2011. Roles of beta-catenin signaling in phenotypic expression and proliferation of articular cartilage superficial zone cells. Lab Invest 91(12):1739-52. [PubMed: 21968810]  [MGI Ref ID J:180101]

Yeung J; Esposito MT; Gandillet A; Zeisig BB; Griessinger E; Bonnet D; So CW. 2010. beta-Catenin mediates the establishment and drug resistance of MLL leukemic stem cells. Cancer Cell 18(6):606-18. [PubMed: 21156284]  [MGI Ref ID J:167611]

Yin Y; White AC; Huh SH; Hilton MJ; Kanazawa H; Long F; Ornitz DM. 2008. An FGF-WNT gene regulatory network controls lung mesenchyme development. Dev Biol 319(2):426-36. [PubMed: 18533146]  [MGI Ref ID J:137691]

Yu Q; Quinn WJ 3rd; Salay T; Crowley JE; Cancro MP; Sen JM. 2008. Role of beta-catenin in B cell development and function. J Immunol 181(6):3777-83. [PubMed: 18768830]  [MGI Ref ID J:139115]

Yuasa T; Kondo N; Yasuhara R; Shimono K; Mackem S; Pacifici M; Iwamoto M; Enomoto-Iwamoto M. 2009. Transient activation of Wnt/{beta}-catenin signaling induces abnormal growth plate closure and articular cartilage thickening in postnatal mice. Am J Pathol 175(5):1993-2003. [PubMed: 19815716]  [MGI Ref ID J:154696]

Zacharias AL; Gage PJ. 2010. Canonical Wnt/beta-catenin signaling is required for maintenance but not activation of Pitx2 expression in neural crest during eye development. Dev Dyn 239(12):3215-25. [PubMed: 20960542]  [MGI Ref ID J:166528]

Zamora M; Manner J; Ruiz-Lozano P. 2007. Epicardium-derived progenitor cells require beta-catenin for coronary artery formation. Proc Natl Acad Sci U S A 104(46):18109-14. [PubMed: 17989236]  [MGI Ref ID J:127444]

Zhang T; Liu S; Yang P; Han C; Wang J; Liu J; Han Y; Yu Y; Cao X. 2009. Fibronectin maintains survival of mouse natural killer (NK) cells via CD11b/Src/beta-catenin pathway. Blood 114(19):4081-8. [PubMed: 19738028]  [MGI Ref ID J:154182]

Zhang Y; Goss AM; Cohen ED; Kadzik R; Lepore JJ; Muthukumaraswamy K; Yang J; DeMayo FJ; Whitsett JA; Parmacek MS; Morrisey EE. 2008. A Gata6-Wnt pathway required for epithelial stem cell development and airway regeneration. Nat Genet 40(7):862-70. [PubMed: 18536717]  [MGI Ref ID J:138407]

Zhang Y; Morris JP 4th; Yan W; Schofield HK; Gurney A; Simeone DM; Millar SE; Hoey T; Hebrok M; Pasca di Magliano M. 2013. Canonical Wnt Signaling Is Required for Pancreatic Carcinogenesis. Cancer Res 73(15):4909-4922. [PubMed: 23761328]  [MGI Ref ID J:199468]

Zhao C; Blum J; Chen A; Kwon HY; Jung SH; Cook JM; Lagoo A; Reya T. 2007. Loss of beta-catenin impairs the renewal of normal and CML stem cells in vivo. Cancer Cell 12(6):528-41. [PubMed: 18068630]  [MGI Ref ID J:130324]

Zhao T; Gan Q; Stokes A; Lassiter RN; Wang Y; Chan J; Han JX; Pleasure DE; Epstein JA; Zhou CJ. 2014. beta-catenin regulates Pax3 and Cdx2 for caudal neural tube closure and elongation. Development 141(1):148-57. [PubMed: 24284205]  [MGI Ref ID J:206311]

Zhou D; Li Y; Lin L; Zhou L; Igarashi P; Liu Y. 2012. Tubule-specific ablation of endogenous beta-catenin aggravates acute kidney injury in mice. Kidney Int 82(5):537-47. [PubMed: 22622501]  [MGI Ref ID J:198173]

Zhou D; Tan RJ; Zhou L; Li Y; Liu Y. 2013. Kidney tubular beta-catenin signaling controls interstitial fibroblast fate via epithelial-mesenchymal communication. Sci Rep 3:1878. [PubMed: 23698793]  [MGI Ref ID J:207805]

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Zhou J; Qu J; Yi XP; Graber K; Huber L; Wang X; Gerdes AM; Li F. 2007. Upregulation of gamma-catenin compensates for the loss of beta-catenin in adult cardiomyocytes. Am J Physiol Heart Circ Physiol 292(1):H270-6. [PubMed: 16936006]  [MGI Ref ID J:119968]

Zou SS; Yang W; Yan HX; Yu LX; Li YQ; Wu FQ; Tang L; Lin Y; Guo LN; Zhou HB; Zhou DX; Shen F; Wu MC; Hu HP; Wang HY. 2013. Role of beta-Catenin in regulating the balance between TNF-alpha- and Fas-induced acute liver injury. Cancer Lett 335(1):160-7. [PubMed: 23410872]  [MGI Ref ID J:198312]

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Health & husbandry

Health & Colony Maintenance Information

Animal Health Reports

Room Number           AX11

Colony Maintenance

Breeding & HusbandryThis strain originated on a B6;129 background and has been backcrossed to C57BL/6J for at least ten generations before being made homozygous. Coat color expected from breeding:Black
Mating SystemHomozygote x Homozygote         (Female x Male)   01-MAR-06
Diet Information LabDiet® 5K52/5K67

Pricing and Purchasing

Pricing, Supply Level & Notes, Controls

Pricing for USA, Canada and Mexico shipping destinations View International Pricing

Live Mice

Price per mouse (US dollars $)GenderGenotypes Provided
Individual Mouse $239.00Female or MaleHomozygous for Ctnnb1tm2Kem  
Price per Pair (US dollars $)Pair Genotype
$478.00Homozygous for Ctnnb1tm2Kem x Homozygous for Ctnnb1tm2Kem  

Standard Supply

Repository-Live represents an exclusive set of over 1800 unique mouse models across a vast array of research areas. Breeding colonies provide mice for large and small orders and fluctuate in size depending on current research demand. If a strain is not immediately available, you will receive an estimated availability timeframe for your inquiry or order in 2-3 business days. Repository strains typically are delivered at 4 to 8 weeks of age. Requests for specific ages will be noted but not guaranteed and we do not accept age requests for breeder pairs. However, if cohorts of mice (5 or more of one gender) are needed at a specific age range for experiments, we will do our best to accommodate your age request.

Pricing for International shipping destinations View USA Canada and Mexico Pricing

Live Mice

Price per mouse (US dollars $)GenderGenotypes Provided
Individual Mouse $310.70Female or MaleHomozygous for Ctnnb1tm2Kem  
Price per Pair (US dollars $)Pair Genotype
$621.40Homozygous for Ctnnb1tm2Kem x Homozygous for Ctnnb1tm2Kem  

Standard Supply

Repository-Live represents an exclusive set of over 1800 unique mouse models across a vast array of research areas. Breeding colonies provide mice for large and small orders and fluctuate in size depending on current research demand. If a strain is not immediately available, you will receive an estimated availability timeframe for your inquiry or order in 2-3 business days. Repository strains typically are delivered at 4 to 8 weeks of age. Requests for specific ages will be noted but not guaranteed and we do not accept age requests for breeder pairs. However, if cohorts of mice (5 or more of one gender) are needed at a specific age range for experiments, we will do our best to accommodate your age request.

View USA Canada and Mexico Pricing View International Pricing

Standard Supply

Repository-Live represents an exclusive set of over 1800 unique mouse models across a vast array of research areas. Breeding colonies provide mice for large and small orders and fluctuate in size depending on current research demand. If a strain is not immediately available, you will receive an estimated availability timeframe for your inquiry or order in 2-3 business days. Repository strains typically are delivered at 4 to 8 weeks of age. Requests for specific ages will be noted but not guaranteed and we do not accept age requests for breeder pairs. However, if cohorts of mice (5 or more of one gender) are needed at a specific age range for experiments, we will do our best to accommodate your age request.

Control Information

   000664 C57BL/6J
  Considerations for Choosing Controls
  Control Pricing Information for Genetically Engineered Mutant Strains.

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The Jackson Laboratory's Genotype Promise

The Jackson Laboratory has rigorous genetic quality control and mutant gene genotyping programs to ensure the genetic background of JAX® Mice strains as well as the genotypes of strains with identified molecular mutations. JAX® Mice strains are only made available to researchers after meeting our standards. However, the phenotype of each strain may not be fully characterized and/or captured in the strain data sheets. Therefore, we cannot guarantee a strain's phenotype will meet all expectations. To ensure that JAX® Mice will meet the needs of individual research projects or when requesting a strain that is new to your research, we suggest ordering and performing tests on a small number of mice to determine suitability for your particular project.
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JAX® Mice, Products & Services Conditions of Use

"MICE" means mouse strains, their progeny derived by inbreeding or crossbreeding, unmodified derivatives from mouse strains or their progeny supplied by The Jackson Laboratory ("JACKSON"). "PRODUCTS" means biological materials supplied by JACKSON, and their derivatives. "RECIPIENT" means each recipient of MICE, PRODUCTS, or services provided by JACKSON including each institution, its employees and other researchers under its control. MICE or PRODUCTS shall not be: (i) used for any purpose other than the internal research, (ii) sold or otherwise provided to any third party for any use, or (iii) provided to any agent or other third party to provide breeding or other services. Acceptance of MICE or PRODUCTS from JACKSON shall be deemed as agreement by RECIPIENT to these conditions, and departure from these conditions requires JACKSON's prior written authorization.

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In case of dissatisfaction for a valid reason and claimed in writing by a purchaser within ninety (90) days of receipt of mice, products or services, JACKSON will, at its option, provide credit or replacement for the mice or product received or the services provided.

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In no event shall JACKSON, its trustees, directors, officers, employees, and affiliates be liable for any causes of action or damages, including any direct, indirect, special, or consequential damages, arising out of the provision of MICE, PRODUCTS or services, including economic damage or injury to property and lost profits, and including any damage arising from acts or negligence on the part of JACKSON, its agents or employees. Unless prohibited by law, in purchasing or receiving MICE, PRODUCTS or services from JACKSON, purchaser or recipient, or any party claiming by or through them, expressly releases and discharges JACKSON from all such causes of action or damages, and further agrees to defend and indemnify JACKSON from any costs or damages arising out of any third party claims.

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The foregoing represents the General Terms and Conditions applicable to JACKSON’s MICE, PRODUCTS or services. In addition, special terms and conditions of sale of certain MICE, PRODUCTS or services may be set forth separately in JACKSON web pages, catalogs, price lists, contracts, and/or other documents, and these special terms and conditions shall also govern the sale of these MICE, PRODUCTS and services by JACKSON, and by its licensees and distributors.

Acceptance of delivery of MICE, PRODUCTS or services shall be deemed agreement to these terms and conditions. No purchase order or other document transmitted by purchaser or recipient that may modify the terms and conditions hereof, shall be in any way binding on JACKSON, and instead the terms and conditions set forth herein, including any special terms and conditions set forth separately, shall govern the sale of MICE, PRODUCTS or services by JACKSON.