- decreased circulating serum albumin level / IMPC
- decreased prepulse inhibition / IMPC
- small spleen / IMPC
- hypoplasia / IMPC
- increased grip strength / IMPC
- abnormal ovary morphology / IMPC
- neoplasia / IMPC
- abnormal liver morphology / IMPC
- abnormal uterus morphology / IMPC
- abnormal thymus morphology / IMPC
- abnormal bone structure / IMPC
- short tibia / IMPC
- small kidney / IMPC
- decreased body length / IMPC
- preweaning lethality, incomplete penetrance / IMPC
- absent adrenal gland / IMPC
- small adrenal glands / IMPC
- abnormal sternum morphology / IMPC
- decreased bone mineral density / IMPC
- hyperactivity / IMPC
- abnormal lung morphology / IMPC
- small uterus / IMPC
- enlarged lymph nodes / IMPC
- decreased exploration in new environment / IMPC
- decreased circulating total protein level / IMPC
- decreased bone mineral content / IMPC
C57BL/6N-Adnp2em1Wtsi/WtsiH
| Status | Available to order |
| EMMA ID | EM:13528 |
| Citation information | RRID:IMSR_EM:13528 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-Adnp2em1Wtsi/WtsiH |
| Alternative name | Adnptm1.1Wtsi |
| Strain type | Endonuclease-mediated |
| Allele/Transgene symbol | Adnp2em1Wtsi |
| Gene/Transgene symbol | Adnp2 |
Information from provider
| Provider | Wellcome Trust Sanger Institute |
| Provider affiliation | Wellcome Trust Sanger Institute |
| Genetic information | Adnp2a_GFP_H2b. KO first WT function activated by cre excision of cassettte. Pre flp excision of selectable marker. Note: ES cells were generated using the CRISPR/Cas9 technology. The details of the applied experimental procedures involving CRISPR/Cas9 technology are not available. |
| Phenotypic information | Homozygous:data not availableHeterozygous:data not available |
| Breeding history | Chimeras crossed with C57BL/6N then crossed with C57BL/6N |
| References | None available |
| Homozygous fertile | not known |
| Homozygous viable | not known |
| Homozygous matings required | not known |
| Immunocompromised | not known |
Information from EMMA
| Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
IMPC phenotypes (gene matching)
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