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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Prf1tm1Tsc
targeted mutation 1, Jurg Tschopp
MGI:2158418
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Prf1tm1Tsc/Prf1tm1Tsc 129X1.129S2-Prf1tm1Tsc MGI:4354612
hm2
Prf1tm1Tsc/Prf1tm1Tsc involves: 129S2/SvPas MGI:4354595
ht3
Prf1tm1Tsc/Prf1+ involves: 129S2/SvPas MGI:4354596


Genotype
MGI:4354612
hm1
Allelic
Composition
Prf1tm1Tsc/Prf1tm1Tsc
Genetic
Background
129X1.129S2-Prf1tm1Tsc
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Prf1tm1Tsc mutation (0 available); any Prf1 mutation (48 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice challenged with RMAS or B16 tumors exhibit increased lethality compared with similarly treated wild-type mice

immune system
• NK and CD8+ T cell death in the tumor ascites from mice transplanted with RMAS cells is decreased compared to that of similarly treated wild-type mice and further decreased after T reg depletion
• NK and CD8+ T cell death in the tumor ascites from mice transplanted with RMAS cells is decreased compared to that of similarly treated wild-type mice and further decreased after T reg depletion

neoplasm
• tumor burden in mice challenged with RMAS cells is increased compared to in similarly treated wild-type mice

cellular
• NK and CD8+ T cell death in the tumor ascites from mice transplanted with RMAS cells is decreased compared to that of similarly treated wild-type mice and further decreased after T reg depletion

hematopoietic system
• NK and CD8+ T cell death in the tumor ascites from mice transplanted with RMAS cells is decreased compared to that of similarly treated wild-type mice and further decreased after T reg depletion
• NK and CD8+ T cell death in the tumor ascites from mice transplanted with RMAS cells is decreased compared to that of similarly treated wild-type mice and further decreased after T reg depletion




Genotype
MGI:4354595
hm2
Allelic
Composition
Prf1tm1Tsc/Prf1tm1Tsc
Genetic
Background
involves: 129S2/SvPas
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Prf1tm1Tsc mutation (0 available); any Prf1 mutation (48 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• despite inducing some signs of apoptosis, mice fail to mount a significant cytotoxic T lymphocyte response to target cells unlike similarly treated wild-type mice
• however, an excess of cytolytic cells promotes lysis and exocytosis of cytotoxic granules is normal following incubation with immobilized anti-CD3 antibodies
• mice exhibit reduced Pseudomonas aerugiosa exotoxin-induced liver damage compared with similarly treated wild-type mice

homeostasis/metabolism
• following exposure to Pseudomonas aerugiosa exotoxin

hematopoietic system
• despite inducing some signs of apoptosis, mice fail to mount a significant cytotoxic T lymphocyte response to target cells unlike similarly treated wild-type mice
• however, an excess of cytolytic cells promotes lysis and exocytosis of cytotoxic granules is normal following incubation with immobilized anti-CD3 antibodies




Genotype
MGI:4354596
ht3
Allelic
Composition
Prf1tm1Tsc/Prf1+
Genetic
Background
involves: 129S2/SvPas
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Prf1tm1Tsc mutation (0 available); any Prf1 mutation (48 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• 2-fold lower compared to wild-type cells
• cytotoxic T lymphocyte activity is slightly lower than in similarly treated wild-type mice
• however, exocytosis of cytotoxic granules is normal following incubation with immobilized anti-CD3 antibodies

hematopoietic system
• 2-fold lower compared to wild-type cells
• cytotoxic T lymphocyte activity is slightly lower than in similarly treated wild-type mice
• however, exocytosis of cytotoxic granules is normal following incubation with immobilized anti-CD3 antibodies





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last database update
05/07/2024
MGI 6.23
The Jackson Laboratory