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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Crbntm1.2Jjh
targeted mutation 1.2, Joseph Higgins
MGI:5302192
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Crbntm1.2Jjh/Crbntm1.2Jjh involves: C57BL/6 MGI:5302204


Genotype
MGI:5302204
hm1
Allelic
Composition
Crbntm1.2Jjh/Crbntm1.2Jjh
Genetic
Background
involves: C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Crbntm1.2Jjh mutation (0 available); any Crbn mutation (33 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
N
• mice exhibit normal basal locomotion and anxiety-like behaviors (J:179427)
• mice exhibit normal social behavior in the three-chamber social interaction and social preference tests and no differences in repetitive grooming behavior (J:259276)
• mice freeze significantly less than control mice in a contextual fear conditioning task, indicating deficit it associative learning (J:179427)
• in a test for contextual fear memory, mice freeze less than wild-type mice (J:259276)
• treatment with Compound C, rescues the contextual fear memory defect (J:259276)
• in the Morris water maze, mice take longer to locate the submerged platform during training indicating a deficit in learning
• in the water-based Y-maze task, mice take longer to locate the platform during training
• treatment with Compound C, a specific inhibitor of AMPK, rescues the learning deficits seen in the Y maze
• mice do not spend more time in the goal zone as seen in wild-type mice at 48 hours following the final training session in the Morris water maze, indicating impaired long-term memory
• during the memory test of the Y-maze, mice take longer to locate the platform, indicating impaired long-term memory
• however, no difference in percentage of spontaneous alternations is seen indicating normal working memory
• treatment with Compound C, a specific inhibitor of AMPK, rescues the memory deficits seen in the Y maze

nervous system
N
• brains have normal gross morphology at postnatal week 8
• marker analysis indicates an imbalance between excitatory and inhibitory synapses with higher markers of presynaptic and postsynaptic glutamatergic spines but lower levels of postsynaptic glutamatergic proteins
• mice exhibit a deficit in hippocampal long-term potentiation compared to wild-type mice

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
autosomal recessive intellectual developmental disorder DOID:0060308 OMIM:PS249500
J:259276





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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory