About   Help   FAQ
Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Lrsam1Gt(RRK461)Byg
gene trap RRK461, BayGenomics
MGI:4329496
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Lrsam1Gt(RRK461)Byg/Lrsam1Gt(RRK461)Byg involves: 129P2/OlaHsd MGI:5496257
ht2
Lrsam1Gt(RRK461)Byg/Lrsam1+ involves: 129P2/OlaHsd MGI:5496260


Genotype
MGI:5496257
hm1
Allelic
Composition
Lrsam1Gt(RRK461)Byg/Lrsam1Gt(RRK461)Byg
Genetic
Background
involves: 129P2/OlaHsd
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Lrsam1Gt(RRK461)Byg mutation (1 available); any Lrsam1 mutation (32 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• number of axons in the motor branch of the femoral nerve is slightly reduced at >12 months of age compared to controls, although cross-sectional area of axons is unchanged
• average axon diameter in the sensory branch of the femoral nerve is slightly increased at >12 months of age compared to controls
• 5 month old mice treated with the neurotoxic agent acrylamide have reduced axon cross-sectional areas in the motor branch of the femoral nerve, suggesting a loss of large diameter axons
• area of neuromuscular junction of the tibialis anterior muscle is increased at 5 months of age, but is similar to control at > 12 months of age
• peripheral motor axons exhibit increased sensitivity to acrylamide-induced degeneration
• untreated mice exhibit modest differences in neuromuscular junction area and axon number
• decrease in nerve conduction velocity is observed in 5 month old mice treated with the neurotoxic agent acrylamide for two weeks

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
Charcot-Marie-Tooth disease axonal type 2P DOID:0110169 OMIM:614436
J:196447




Genotype
MGI:5496260
ht2
Allelic
Composition
Lrsam1Gt(RRK461)Byg/Lrsam1+
Genetic
Background
involves: 129P2/OlaHsd
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Lrsam1Gt(RRK461)Byg mutation (1 available); any Lrsam1 mutation (32 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• paws turn outward
• wider stance than control, however gait, stride time, stance time and swing time are similar to control

nervous system
• number of axons in the motor branch of the femoral nerve is slightly reduced at >12 months of age compared to controls, although cross-sectional area of axons is unchanged
• average axon diameter in the sensory branch of the femoral nerve is slightly decreased at >12 months of age compared to controls
• number of motor axons in the femoral nerve are reduced in 5 month old mice treated with the neurotoxic agent acrylamide
• area of neuromuscular junction in the bone region of the tibialis anterior muscle is increased at 5 months of age, but is similar to control at > 12 months of age





Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
05/07/2024
MGI 6.23
The Jackson Laboratory