- 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
B6;129-Prdm8tm1Mci/H
| Status | Available to order |
| EMMA ID | EM:12207 |
| Citation information | RRID:IMSR_EM:12207 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;129-Prdm8tm1Mci/H |
| Alternative name | Prdm8-eGFP knock in (Background=50%C57BL/6J; 25% 129S1/SviMJ; 25% 129X1/SvJ) |
| Strain type | Targeted Mutant Strains : Knock-out |
| Allele/Transgene symbol | Prdm8tm1Mci |
| Gene/Transgene symbol | Prdm8 |
Information from provider
| Provider | Rod McInnes |
| Provider affiliation | Lady Davis Research Institute, McGill University |
| Additional owner | Prof. Rod McInnes, Lady Davis Research Institute, Montreal, Canada |
| Genetic information | GFP knock-in replacing the second coding exon and part of the third coding exon of the Prdm8 gene, using an IRES-EGFPnls/DTA-Neo reporter/selection cassette. |
| Phenotypic information | Homozygous:Homozygous mice have a night blindness phenotype due to the loss of retinal rod bipolar cells (Jung, Atan et al. PNAS 2015).Heterozygous:Heterozygous mice are identical to wild-type. |
| Breeding history | Maintained on mixed background (50% C57BL/6J; 25% 129S1/SviMJ; 25% 129X1/SvJ). |
| References |
|
| Homozygous fertile | no |
| Homozygous viable | yes |
| Homozygous matings required | no |
| 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)
Literature references
- Transcription factor PRDM8 is required for rod bipolar and type 2 OFF-cone bipolar cell survival and amacrine subtype identity.;Jung Cynthia C, Atan Denize, Ng David, Ploder Lynda, Ross Sarah E, Klein Martin, Birch David G, Diez Eduardo, McInnes Roderick R, ;2015;Proceedings of the National Academy of Sciences of the United States of America;112;E3010-9; 26023183
- Bhlhb5 and Prdm8 form a repressor complex involved in neuronal circuit assembly.;Ross Sarah E, McCord Alejandra E, Jung Cynthia, Atan Denize, Mok Stephanie I, Hemberg Martin, Kim Tae-Kyung, Salogiannis John, Hu Linda, Cohen Sonia, Lin Yingxi, Harrar Dana, McInnes Roderick R, Greenberg Michael E, ;2012;Neuron;73;292-303; 22284184
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