- abnormal head morphology / IMPC
- abnormal snout morphology / IMPC
- decreased body length / IMPC
- decreased startle reflex / IMPC
- short tibia / IMPC
- abnormal bone structure / IMPC
- abnormal auditory brainstem response / IMPC
- increased circulating aspartate transaminase level / IMPC
- increased grip strength / IMPC
- increased red blood cell distribution width / IMPC
- decreased CD8-positive, naive alpha-beta T cell number / IMPC
- hyperplasia / IMPC
C57BL/6NCrl-Plag1em1(IMPC)Hmgu/Ieg
Status | Available to order |
EMMA ID | EM:13491 |
Citation information | RRID:IMSR_EM:13491 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/6NCrl-Plag1em1(IMPC)Hmgu/Ieg |
Alternative name | |
Strain type | Endonuclease-mediated |
Allele/Transgene symbol | Plag1em1(IMPC)Hmgu |
Gene/Transgene symbol | Plag1 |
Information from provider
Provider | Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH) |
Provider affiliation | Institute of Experimental Genetics, Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH) |
Genetic information | This mouse line originates from CRISPR zygote microinjection. For further details see the project page at the IMPC portal. |
Phenotypic information | Potential phenotyping data in the IMPC portal |
References | None available |
Information from EMMA
Archiving centre | Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH), Oberschleißheim, Germany |
Animals used for archiving | heterozygous C57BL/6N males |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Silver-Russell syndrome due to a point mutation / Orphanet_397590
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- short tibia / IMPC
- decreased CD8-positive, naive alpha-beta T cell number / IMPC
- abnormal snout morphology / IMPC
- abnormal head morphology / IMPC
- hyperplasia / IMPC
- increased red blood cell distribution width / IMPC
- increased grip strength / IMPC
- abnormal bone structure / IMPC
- decreased body length / IMPC
- increased circulating aspartate transaminase level / IMPC
- decreased startle reflex / IMPC
- abnormal auditory brainstem response / IMPC
Information on how we integrate external resources can be found here
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