- absent seminal vesicle / IMPC
- preweaning lethality, incomplete penetrance / IMPC
- enlarged seminal vesicle / IMPC
- abnormal uterus morphology / IMPC
- no spontaneous movement / IMPC
- enlarged spleen / IMPC
- small testis / IMPC
- abnormal kidney morphology / IMPC
- decreased heart rate / IMPC
- abnormal testis morphology / IMPC
- abnormal liver morphology / IMPC
- blind uterus / IMPC
- small kidney / IMPC
- abnormal spleen morphology / IMPC
- prolonged RR interval / IMPC
C57BL/6N-Chmp2btm1.1Ics/Ics
| Status | Available to order |
| EMMA ID | EM:16210 |
| Citation information | RRID:IMSR_EM:16210 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 | C57BL/6N-Chmp2btm1.1Ics/Ics |
| Alternative name | Chmp2btm1.1Ics/Ics |
| Strain type | Targeted Mutant Strains : Knock-in |
| Allele/Transgene symbol | Chmp2btm1.1Ics |
| Gene/Transgene symbol | Chmp2b |
Information from provider
| Provider | Frédérique Rene |
| Provider affiliation | Centre de Recherche en Biomédecine de Strasbourg (CRBS) |
| Genetic information | We inserted into intron 4 a loxP site, the exon 5 sequence (ENSMUSE00000131914, Chmp2b-201 GRCm39), a STOP codon, an IRES sequence, the eYFP reporter sequence and a 3X pA sequence followed by a FRT-flanked neomycin resistance gene cassette and a second loxP site. The neo cassette was removed through subsequent flp-mediated recombination leading to a knock-in reporter allele of Chmp2b which can be reverted to a wild-type allele upon cre-mediated recombination. |
| Phenotypic information | Homozygous:N/AHeterozygous:N/A |
| Breeding history | 100% C57BL/6N (C57BL/6NCrl 99,22% C57BL/6NTac 0,78%) |
| References | None available |
| Homozygous fertile | not known |
| Homozygous viable | not known |
| Homozygous matings required | no |
| Immunocompromised | no |
Information from EMMA
| Archiving centre | ICS, Institut Clinique de la Souris, Illkirch-Graffenstaden, France |
Disease and phenotype information
IMPC phenotypes (gene matching)
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