Phenotypes associated with this allele
|
Find Mice |
Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ssttm2.1(cre)Zjh mutation
(4 available);
any
Sst mutation
(35 available)
|
|
|
normal phenotype
|
• homozygous mice are viable, fertile, normal in size and do not display any gross physical or behavioral abnormalities
|
mortality/aging
|
• 50% mortality by 29-35 weeks of age
|
behavior/neurological
|
• mice exhibit repetitive nose-poking behavior in the hole board test
• however, mice do not exhibit motor deficits or alternations in acoustic startle response, partition, or cued memory tests, or differences in anxiety, pre-pulse inhibition, locomotor activity or long-term potentiation
|
|
• 50% of mice develop spontaneous epileptic seizures starting at 12 weeks
|
|
• mice show generalized tonic clonic seizures during routine handling
|
nervous system
|
• 50% of mice develop spontaneous epileptic seizures starting at 12 weeks
|
|
• mice show generalized tonic clonic seizures during routine handling
|
behavior/neurological
N |
• mice exhibit normal hypertonia and no hyper-aggression
|
|
• attention deficits as in knock-out mice
|
|
• highly fragmented sleep
|
behavior/neurological
|
• mice infusion with asunaprivir (drug inducer of iPKR) exhibit reduced memory in a cued threat-conditioning paradigm compared with wild-type
|
|
Find Mice |
Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Col1a1tm1(tetO-GFP,-RNAi:Eef1a1)Mcg mutation
(0 available);
any
Col1a1 mutation
(160 available)
Ssttm2.1(cre)Zjh mutation
(4 available);
any
Sst mutation
(35 available)
|
|
|
behavior/neurological
N |
• mice virally expressing a cre-dependent tet transactivator exhibit normal behavior in an open field and exploration of an elevated plus maze
|
|
• mice virally expressing a cre-dependent tet transactivator exhibit reduced long term memory in a cued threat-conditioning paradigm compared with wild-type
• however, supplementation with doxycycline rescues phenotype
|