- 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 |
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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