About   Help   FAQ
Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Trpm2tm1Yamo
targeted mutation 1, Yasuo Mori
MGI:3803341
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Trpm2tm1Yamo/Trpm2tm1Yamo B6J.129S4-Trpm2tm1Yamo MGI:5697656
hm2
Trpm2tm1Yamo/Trpm2tm1Yamo involves: 129S4/SvJae * C57BL/6J MGI:3804476


Genotype
MGI:5697656
hm1
Allelic
Composition
Trpm2tm1Yamo/Trpm2tm1Yamo
Genetic
Background
B6J.129S4-Trpm2tm1Yamo
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Trpm2tm1Yamo mutation (0 available); any Trpm2 mutation (109 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• the anti-manic action of lithium on amphetamine-induced hyperactivity is completely absent in mutants
• mice spend less time in the open arms of the elevated plus maze, indicating increased anxiety
• in the light/dark transition task, mice show a longer latency to the light chamber, although mice spend similar amounts of time in each changer as wild-type mice
• in social investigation of an anesthetized mouse target, mutants spend much less time in contact with the target compared to wild-type mice, however there is no difference in the latency to first contact or in the number of contacts with the target
• in a social interaction task in which mice are presented with an unfamiliar juvenile mouse, mutants show a reduction in social interaction time
• on the sociability test, no difference is seen in the amount of time that mutants spend in the two chambers, however mutants spend less time sniffing a stranger 1 mouse cage than the wild-type mice
• in the subsequent social novelty preference test, mutants spend similar amount of time in the two chambers, however mutants spend less time in sniffing the stranger 2 mouse cage than wild-type mice
• in the resident-intruder task, mutants show a similar number of attacks as wild-type mice, indicating normal aggressive behavior

nervous system
• EEG signals from the frontal and parietal cortices show a decrease in entropy at different thresholds from those of wild-type mice, indicating increased regularity or decreased complexity in the EEG signals
• EEG signals show lower correlation coefficients between the frontal and parietal cortices in the alpha, beta, and gamma-frequency ranges, indicating decreased EEG synchronization between the two regions
• mice show lower coherence values between the frontal and parietal cortices, indicating a weaker association between the two regions in mutants




Genotype
MGI:3804476
hm2
Allelic
Composition
Trpm2tm1Yamo/Trpm2tm1Yamo
Genetic
Background
involves: 129S4/SvJae * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Trpm2tm1Yamo mutation (0 available); any Trpm2 mutation (109 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• decrease in the number of neutrophils recruited following dextran sulfate sodium treatment
• however, no defects in neutrophil migration are detected in vitro
• absence of ADP-ribose- and near absence of H2O2-evoked cationic currents
• impaired expression of CXCL2 in response to H2O2 or endotoxin lipopolysacharide and tumor necrosis factor alpha
• suppression of increase in IFNG levels in the colon induced by dextran sulfate sodium
• suppression of increase in IL12 levels in the colon induced by dextran sulfate sodium
• in a dextran sulfate sodium-induced model of colitis expression of interferon gamma and interleukin 12 is suppressed, the number of recruited neutrophils is decreased, weight loss and colon shortening are not detected and the overall severity of colitis is reduced
• however, recruitment of macrophages and expression of other cytokines is unaffected

homeostasis/metabolism
• suppression of increase in IFNG levels in the colon induced by dextran sulfate sodium
• suppression of increase in IL12 levels in the colon induced by dextran sulfate sodium

hematopoietic system
• decrease in the number of neutrophils recruited following dextran sulfate sodium treatment
• however, no defects in neutrophil migration are detected in vitro
• absence of ADP-ribose- and near absence of H2O2-evoked cationic currents
• impaired expression of CXCL2 in response to H2O2 or endotoxin lipopolysacharide and tumor necrosis factor alpha





Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
05/07/2024
MGI 6.23
The Jackson Laboratory