- increased heart rate / IMPC
- increased circulating sodium level / IMPC
- abnormal thymus morphology / IMPC
- enlarged thymus / IMPC
- abnormal retina morphology / IMPC
- hyperactivity / IMPC
- impaired glucose tolerance / IMPC
- decreased locomotor activity / IMPC
- abnormal tooth morphology / IMPC
- decreased body weight / IMPC
- increased prepulse inhibition / IMPC
- increased freezing behavior / IMPC
- abnormal spleen morphology / IMPC
- abnormal skin morphology / IMPC
- abnormal seminal vesicle morphology / IMPC
- abnormal heart left ventricle morphology / IMPC
- increased airway resistance / IMPC
- small heart / IMPC
- small spleen / IMPC
- abnormal inspiratory capacity / IMPC
- abnormal uterus morphology / IMPC
- abnormal heart morphology / IMPC
- increased anxiety-related response / IMPC
- enlarged uterus / IMPC
- increased lung elastance / IMPC
C57BL/6NTac-Prdm8em1H/H
Status | Available to order |
EMMA ID | EM:13023 |
Citation information | RRID:IMSR_EM:13023 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/6NTac-Prdm8em1H/H |
Alternative name | Prdm8-FLOX-EM1-B6N |
Strain type | Endonuclease-mediated |
Allele/Transgene symbol | Prdm8em1H |
Gene/Transgene symbol | Prdm8 |
Information from provider
Provider | MRC-Harwell |
Provider affiliation | Mary Lyon Centre at MRC Harwell |
Genetic information | For detailed information on the genetic description of this strain, please have a look at this report. |
Phenotypic information | Homozygous:Unkown at this stage - are breeding homs currentlyHeterozygous:None |
Breeding history | Co-isogenic on original background |
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
Orphanet associated rare diseases, based on orthologous gene matching
- Early-onset Lafora body disease / Orphanet_324290
IMPC phenotypes (gene matching)
Information on how we integrate external resources can be found here
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