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Phenotypes Associated with This Genotype
Genotype
MGI:3795243
Allelic
Composition
Cnr1tm1Zim/Cnr1tm1Zim
Genetic
Background
involves: 129 * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cnr1tm1Zim mutation (2 available); any Cnr1 mutation (43 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• over time, mutants show an increase in spontaneous deaths, with more than 30% of mutants under 24 weeks of age dying
• over time, mutants show an increase in spontaneous deaths, with more than 30% of mutants under 24 weeks of age dying
• death is sudden with no signs of weight loss, dehydration, or abnormal posture
• fewer than the expected numbers (23.3% vs. 29% expected) of homozygotes are seen at weaning, indicating some loss either during embryonic development or early postnatal life

reproductive system
• mice exhibit preterm labor prior to day 19.6 of pregnancy compared with wild-type mice

behavior/neurological
• mutants show no hypothermia, no hypoactivity, and no catalepsy after administration of HU210, a potent synthetic cannabinoid agonist or delta9-tetrahydrocannabinol (THC) and no delta9-THC-induced analgesia in the hotplate test
• mutants exhibit head bobbing, assume a hunched position after injection, lick their abdomens, and have strong diarrhea after delta9-THC injection, unlike wild-type which show pronounced hypoactivity
• rearing rate is reduced drastically
• mutants are hypoactive in the open-field test (J:54995)
• mutants exhibit a reduction in locomotor activity, in both ambulation counts and ambulation time (J:55294)
• however, motor coordination on the rotarod appears normal (J:55294)
• hypoalgesia in hotplate and formalin tests
• responses are normal in the tail-flick test
• mutants show a reduced number of pain responses in the early phase of the formalin test
• mutants show increased response latencies in the hotplate test
• mutants spend longer time motionless in the ring catalepsy test compared to wild-type indicating an increase in ring catalepsy

homeostasis/metabolism
• on days 16 to 19 of pregnancy
• on days 14 to 16 of pregnancy
• on day 19 of pregnancy

cellular
• newborns exhibit reduced birth weights compared to wild-type mice or newborns from homozygous females mated with wild-type mice
• however, treatment with a CRH-RI selective antagonist, antalarmin hydrochloride, on days 15 to 17 of pregnancy or progesterone on day 18 of pregnancy restores normal birth weights


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)
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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory