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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Grin2ctm1Nak
targeted mutation 1, Shigetada Nakanishi
MGI:1928510
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Grin2ctm1Nak/Grin2ctm1Nak involves: 129S/SvEv MGI:4360541
cx2
Grin2atm1Nak/Grin2atm1Nak
Grin2ctm1Nak/Grin2ctm1Nak
involves: 129S/SvEv MGI:4360543


Genotype
MGI:4360541
hm1
Allelic
Composition
Grin2ctm1Nak/Grin2ctm1Nak
Genetic
Background
involves: 129S/SvEv
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Grin2ctm1Nak mutation (1 available); any Grin2c mutation (56 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
N
• no gross anatomical changes in the brain; the organization of the cerebellum is unaltered and the size and density of the granule cells is similar in mutant and control mice
• the rise time in evoked ESPCs is similar in mutant mice compared to controls, but the decay time is faster in mutant mice; the time constants of both fast and slow components of decay decreased in mutant mice compared to controls
• there is no difference in horizontal locomotor activity compared to controls
• the amplitude of the slow component (characteristic of NMDA receptor activity) of spontaneous ESPCs in cerebellar granule cells is reduced by approximately half in mutant mice compared to controls

behavior/neurological
N
• mutant mice do not exhibit ataxia or tremors, and grip strength and righting reflex is similar to controls
• mutant mice do not exhibit impaired coordination in the fixed bar or rotarod tests
• the amount of rearing activity is slightly reduced in mutant mice compared to controls




Genotype
MGI:4360543
cx2
Allelic
Composition
Grin2atm1Nak/Grin2atm1Nak
Grin2ctm1Nak/Grin2ctm1Nak
Genetic
Background
involves: 129S/SvEv
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Grin2atm1Nak mutation (7 available); any Grin2a mutation (66 available)
Grin2ctm1Nak mutation (1 available); any Grin2c mutation (56 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
N
• no gross anatomical changes in the brain; the organization of the cerebellum is unaltered and the size and density of the granule cells is similar in mutant and control mice
• evoked ESPCs are absent in cerebellar granule cells in double mutant mice
• the amplitude of the slow component (characteristic of NMDA receptor activity) of spontaneous ESPCs in cerebellar granule cells is nearly absent in mutant mice compared to controls

behavior/neurological
N
• mutant mice do not exhibit ataxia or tremors, and grip strength and righting reflex is similar to controls
• double mutant mice do not maintain balance and cannot stand or walk on a 6mm wide fixed bar while control mice can walk smoothly and stay on the bar
• on a 20mm fixed bar, mutant mice can can walk smoothly and stay on the bar, similar to controls
• on a rotating rod at 25 rpm, mutant mice fail to stay on the rod and do not improve performance with training
• at 10 and 20 rpm, mutant mice perform similar to controls
• the amount of rearing activity is significantly reduced in mutant mice compared to controls
• there is no difference in horizontal locomotor activity compared to controls





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