- lymphoid hyperplasia / MGI
- enlarged spleen / MGI
- spleen hyperplasia / MGI
- small thymus / MGI
- small testis / MGI
- seminiferous tubule degeneration / MGI
- skin lesions / MGI
- decreased body size / MGI
- male infertility / MGI
- premature death / MGI
- increased susceptibility to viral infection / MGI
- chronic inflammation / MGI
- abnormal epididymis morphology / MGI
- oligozoospermia / MGI
- decreased B cell proliferation / MGI
- decreased T cell proliferation / MGI
- impaired glucose tolerance / MGI
- increased CD4-positive, alpha beta T cell number / MGI
- decreased CD8-positive, alpha-beta T cell number / MGI
- myeloid hyperplasia / MGI
- prenatal lethality, incomplete penetrance / MGI
- decreased pancreatic beta cell proliferation / MGI
C57BL/6N-Ppm1dtm1.2(IMPC)Wtsi/WtsiH
Status | Available to order |
EMMA ID | EM:13529 |
Citation information | RRID:IMSR_EM:13529 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-Ppm1dtm1.2(IMPC)Wtsi/WtsiH |
Alternative name | Ppm1dtm1.2(IMPC)Wtsi (TBXX) |
Strain type | Targeted Mutant Strains : Knock-in |
Allele/Transgene symbol | Ppm1dtm1.2(IMPC)Wtsi |
Gene/Transgene symbol | Ppm1d |
Information from provider
Provider | Wellcome Trust Sanger Institute |
Provider affiliation | Wellcome Trust Sanger Institute |
Genetic information | Ppm1dtm1.2(IMPC)Wtsi. KI replacing exon 6 with a human codon optimised exon 6 followed by a stop cassette and human codon optimised point mutated exon 6 resulting in deletion of T Chr 11:85345824 cause a premature stop codon at L476stop. Post flp deletion of selectable marker |
Phenotypic information | Homozygous:data not availableHeterozygous:data not available |
Breeding history | Chimeras crossed with C57BL/6N then hets crossed with flp on C57BL/6N and crossed with C57BL/6N, then intercrossed |
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
MGI phenotypes (gene matching)
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