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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Lpin120884
20884
MGI:4361554
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Lpin120884/Lpin120884 involves: C57BL/6J MGI:4361557
ht2
Lpin120884/Lpin1fld involves: BALB/cByJ * C57BL/6J MGI:4361559
cx3
Lpin120884/Lpin120884
Nrcam20884/Nrcam20884
involves: C57BL/6J MGI:4361556


Genotype
MGI:4361557
hm1
Allelic
Composition
Lpin120884/Lpin120884
Genetic
Background
involves: C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Lpin120884 mutation (1 available); any Lpin1 mutation (56 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• mild weakness is seen in the hindpaws from about 8 to 12 weeks of age
• hindlimb grip strength is significantly increased compared to controls at 48 weeks of age
• however, forelimb grip strength is normal
• subtle floppy gait that develops between 6 and 9 weeks of age

nervous system
• at 12 weeks of age some axons in the sciatic nerve have thin myelin sheaths
• at 12 weeks of age compact myelin structures are seen beside axons within Schwann cells
• at 52 weeks of age some axons with thin myelin sheaths are still present but the overall state of myelination has improved
• at 8 weeks of age demyelinated axons are present and darkly stained debris is seen in the sciatic nerve
• appear less well organized compared to controls
• at 8 and 12 weeks of age demyelinated axons are present in the sciatic nerve
• at 52 weeks of age some demyelinated axons are still present but the overall state of myelination has improved
• demyelination peaks at 8 weeks of age
• compound muscle action potentials are reduced at 12 weeks of age in the sciatic nerve and the sural nerve
• by 8 weeks of age conduction velocity is reduced in the sciatic nerve and the sural nerve
• decrease is less than in Lpin120884 Nrcam20884 double homozygotes

skeleton
• at 48 weeks of age joint stiffness is seen in the joints of the paws which is associated with an increase in hindpaw grip strength




Genotype
MGI:4361559
ht2
Allelic
Composition
Lpin120884/Lpin1fld
Genetic
Background
involves: BALB/cByJ * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Lpin120884 mutation (1 available); any Lpin1 mutation (56 available)
Lpin1fld mutation (2 available); any Lpin1 mutation (56 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• tendency to clench hindlimbs
• low, floppy gait develops between 6 and 9 weeks of age

nervous system
• axons in sciatic nerves have thin myelin sheaths
• thin myelin sheaths and darkly stained debris are seen




Genotype
MGI:4361556
cx3
Allelic
Composition
Lpin120884/Lpin120884
Nrcam20884/Nrcam20884
Genetic
Background
involves: C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Lpin120884 mutation (1 available); any Lpin1 mutation (56 available)
Nrcam20884 mutation (1 available); any Nrcam mutation (87 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• hindlimb grasping
• at 4 weeks of age hindlimb grip strength is significantly reduced
• at 6 weeks of age half of the mice are unable to grip with their hindpaws
• by 8 weeks of age all of the mice are unable to grip with their hindpaws
• between 32 and 48 weeks of age all mice regain the ability to grip with their hindpaws
• reduced forelimb grip strength is seen at 6 weeks of age, weakness attenuates starting around 24 weeks of age
• develop a floppy gait by 5 weeks of age
• develop hindlimb paralysis by 6 to 7 weeks of age
• paralysis is characterized by partial to total loss of hindlimb joint mobility, inability to grip with the hind paws, and hindlimb grasping when suspended by the tail
• paralysis phenotype attenuates over time
• after 14 weeks of age hindlimbs take on a flaccid disposition and progressively regain mobility and strength
• between 8 months and 1 year of age mice regain the ability to grip structures and walk although the gait remains floppy
• develop hindlimb paralysis by 6 to 7 weeks of age
• paralysis is characterized by partial to total loss of hindlimb joint mobility, inability to grip with the hind paws, and hindlimb grasping when suspended by the tail
• appear to be incapable of suckling pups
• males do not breed

nervous system
• at 12 weeks of age some axons in the sciatic nerve have thin myelin sheaths
• at 12 weeks of age compact myelin structures are seen beside axons within Schwann cells
• at 52 weeks of age some axons with thin myelin sheaths are still present but the overall state of myelination has improved
• at 8 weeks of age demyelinated axons are present and darkly stained debris is seen in the sciatic nerve
• appear less well organized compared to controls
• at 8 and 12 weeks of age demyelinated axons are present in the sciatic nerve
• at 52 weeks of age some demyelinated axons are still present but the overall state of myelination has improved
• demyelination peaks at 8 weeks of age
• compound muscle action potentials are reduced at 8 and 12 weeks of age in the sciatic nerve and the sural nerve
• at 4 and 8 weeks of age conduction velocity is reduced in the sciatic nerve and the sural nerve

muscle
• widespread atrophic fibers are seen in the hindquarters of mice with hindlimb paralysis

skeleton
• at the onset of paralysis joints appear stiff and are restricted to a bent position

growth/size/body
• associated with onset of paralysis and muscle wasting
• body weight recovers in association with attenuation of paralysis and muscle wasting





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last database update
04/30/2024
MGI 6.23
The Jackson Laboratory