Phenotypes associated with this allele
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Find Mice |
Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rgs4tm1Dgen mutation
(1 available);
any
Rgs4 mutation
(18 available)
|
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behavior/neurological
N |
• mice exhibit normal novel object recognition
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• for a scent-paired chamber
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• mice exhibit less social dominance compared with wild-type mice
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Find Mice |
Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rgs4tm1Dgen mutation
(1 available);
any
Rgs4 mutation
(18 available)
|
|
|
adipose tissue
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• 3 of 6 homozygotes at 49 days of age exhibit a high fat percentage
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homeostasis/metabolism
reproductive system
behavior/neurological
N |
• mice exhibit normal social dominance and conditioned place preference
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• mice exhibit reduced novel object recognition compared with wild-type mice
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growth/size/body
N |
• mice exhibit normal weight
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endocrine/exocrine glands
|
Find Mice |
Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Relnctrdel mutation
(0 available);
any
Reln mutation
(209 available)
Rgs4tm1Dgen mutation
(1 available);
any
Rgs4 mutation
(18 available)
|
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nervous system
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• layers II, II, IV, V cannot be distinguished
• brains are otherwise normal
|
|
Find Mice |
Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
m2Bei mutation
(0 available);
any
m2Bei mutation
(0 available)
Rgs4tm1Dgen mutation
(1 available);
any
Rgs4 mutation
(18 available)
|
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nervous system
|
• superficial layers are thinner
|
|
Find Mice |
Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
m3Bei mutation
(0 available);
any
m3Bei mutation
(0 available)
Rgs4tm1Dgen mutation
(1 available);
any
Rgs4 mutation
(18 available)
|
|
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nervous system
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• anterior cortex is sometimes narrow
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• superficial layers are thinner
• layers II, III, IV are disturbed
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mortality/aging
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• postnatal lethality in the third week sometimes
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nervous system
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• severe cortical thinning
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craniofacial
skeleton
|
Find Mice |
Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
m5Bei mutation
(0 available);
any
m5Bei mutation
(0 available)
Rgs4tm1Dgen mutation
(1 available);
any
Rgs4 mutation
(18 available)
|
|
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mortality/aging
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• postnatal lethality in the third week sometimes
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nervous system
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• small
• posteriorly displaced
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• severe cortical thinning
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craniofacial
skeleton
mortality/aging
|
• postnatal lethality in the third week sometimes
|
nervous system
|
• severe cortical thinning
|
craniofacial
skeleton