- decreased prepulse inhibition / IMPC
- decreased body length / IMPC
- decreased fluid intake / IMPC
- decreased bone mineral density / IMPC
- preweaning lethality, complete penetrance / IMPC
- increased startle reflex / IMPC
- increased grip strength / IMPC
- short tibia / IMPC
- decreased bone mineral content / IMPC
- abnormal bone structure / IMPC
B6.Cg-Myctm1.1(MYC)Gwbk/Ieg
| Status | Available to order |
| EMMA ID | EM:06087 |
| Citation information | RRID:IMSR_EM:06087 Research Resource Identifiers (RRID) are persistent unique ID numbers assigned to help researchers cite key resources (e.g. antibodies, model organisms and software projects) in the biomedical literature to improve transparency and reproducibility in research. See https://www.rrids.org/ for more information. |
| International strain name | B6.Cg-Myctm1.1(MYC)Gwbk/Ieg |
| Alternative name | C57BL/6-J / hc-Myc |
| Strain type | Targeted Mutant Strains : Knock-in |
| Allele/Transgene symbol | Myctm1.1(MYC)Gwbk |
| Gene/Transgene symbol | Myc |
Information from provider
| Provider | Georg W. Bornkamm |
| Provider affiliation | Institute of Experimental Genetics, GSF National Research Centre of Environment and Health |
| Genetic information | Humanized c-Myc mouse: targeted knock-in of the human c-MYC gene into the murine c-Myc locus. Human sequences starting at the CTG initiation codon of the first exon. A piece of mouse chromosome 15 (position 61.985.920 to 61.989.995) is replaced by a piece of human chromosome 8 (position 128.748.840 to 128.753.273). |
| Phenotypic information | No obvious phenotype observed. |
| Breeding history | Chimeric mice were backcrossed onto C57BL/6J, followed by mating to C57BL/6J cre deleter mice to remove the neomycin resistance gene. Then backcrossed to C57BL/6J to get rid of the cre deleter construct and brother-sister mating to generate a mouse homozygous for human c-MYC. |
| References |
|
| Homozygous fertile | yes |
| Homozygous viable | yes |
| Homozygous matings required | no |
| Immunocompromised | not known |
Information from EMMA
| Archiving centre | Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH), Oberschleißheim, Germany |
Disease and phenotype information
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- absent erythroid progenitor cell / MGI
- absent common myeloid progenitor cells / MGI
- abnormal vascular development / MGI
- abnormal angiogenesis / MGI
- enlarged heart / MGI
- distended pericardium / MGI
- decreased bone marrow cell number / MGI
- decreased cell proliferation / MGI
- abnormal intestine morphology / MGI
- short tail / MGI
- small lymphoid organs / MGI
- enlarged spleen / MGI
- spleen hypoplasia / MGI
- enlarged lymph nodes / MGI
- abnormal skeletal muscle morphology / MGI
- open neural tube / MGI
- decreased body weight / MGI
- decreased body size / MGI
- cyanosis / MGI
- abnormal vasculogenesis / MGI
- decreased embryo size / MGI
- abnormal embryo turning / MGI
- abnormal placenta morphology / MGI
- placental labyrinth hypoplasia / MGI
- abnormal visceral yolk sac morphology / MGI
- pale yolk sac / MGI
- postnatal growth retardation / MGI
- decreased white adipose tissue amount / MGI
- reduced female fertility / MGI
- decreased litter size / MGI
- increased B cell derived lymphoma incidence / MGI
- decreased tumor incidence / MGI
- premature death / MGI
- no abnormal phenotype detected / MGI
- lymphoid hypoplasia / MGI
- abnormal chorion morphology / MGI
- no phenotypic analysis / MGI
- abnormal intestinal goblet cell morphology / MGI
- embryonic growth retardation / MGI
- spontaneous chromosome breakage / MGI
- induced chromosome breakage / MGI
- decreased fetal size / MGI
- abnormal embryonic erythropoiesis / MGI
- abnormal dorsal aorta morphology / MGI
- abnormal small intestine crypts of Lieberkuhn morphology / MGI
- abnormal large intestine crypts of Lieberkuhn morphology / MGI
- increased spleen weight / MGI
- increased B cell number / MGI
- decreased T cell number / MGI
- abnormal trophoblast layer morphology / MGI
- decreased T cell proliferation / MGI
- increased B cell proliferation / MGI
- abnormal response to injury / MGI
- cardiovascular system phenotype / MGI
- immune system phenotype / MGI
- decreased memory T cell number / MGI
- lymph node hypoplasia / MGI
- decreased small intestinal villus size / MGI
- abnormal T cell receptor beta chain V(D)J recombination / MGI
- increased B cell apoptosis / MGI
- decreased common myeloid progenitor cell number / MGI
- abnormal enterocyte physiology / MGI
- abnormal enterocyte proliferation / MGI
- decreased erythroid progenitor cell number / MGI
- decreased birth weight / MGI
- decreased birth body size / MGI
- abnormal NK cell physiology / MGI
- abnormal intestinal enteroendocrine cell morphology / MGI
- neonatal lethality, incomplete penetrance / MGI
- prenatal lethality, complete penetrance / MGI
- embryonic lethality during organogenesis, complete penetrance / MGI
- decreased fibroblast proliferation / MGI
- absent fibroblast proliferation / MGI
- decreased Paneth cell number / MGI
Literature references
- Humanized c-Myc mouse.;Lehmann Frank M, Feicht Samantha, Helm Florian, Maurberger Anna, Ladinig Camilla, Zimber-Strobl Ursula, Kühn Ralf, Mautner Josef, Gerbitz Armin, Bornkamm Georg W, ;2012;PloS one;7;e42021; 22860051
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