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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Gars1Gt(XM256)6Byg
gene trap 6, BayGenomics
MGI:3655818
Summary 5 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Gars1Gt(XM256)6Byg/Gars1Gt(XM256)6Byg involves: 129P2/OlaHsd * C57BL/6J MGI:3655850
ht2
Gars1Gt(XM256)6Byg/Gars1+ involves: 129P2/OlaHsd * C57BL/6J MGI:3655851
ht3
Gars1Gt(XM256)6Byg/Gars1C201R involves: 129P2/OlaHsd * BALB/cAnN * C3H/HeH * C57BL/6J MGI:5308220
ht4
Gars1Gt(XM256)6Byg/Gars1Nmf249 involves: 129P2/OlaHsd * C57BL/6J MGI:3655852
cx5
Gars1C201R/Gars1Gt(XM256)6Byg
Tg(CAG-GARS)DRwb/0
involves: 129P2/OlaHsd * BALB/cAnN * C3H/HeH * C57BL/6J * FVB/N MGI:5308219


Genotype
MGI:3655850
hm1
Allelic
Composition
Gars1Gt(XM256)6Byg/Gars1Gt(XM256)6Byg
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gars1Gt(XM256)6Byg mutation (0 available); any Gars1 mutation (42 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging




Genotype
MGI:3655851
ht2
Allelic
Composition
Gars1Gt(XM256)6Byg/Gars1+
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gars1Gt(XM256)6Byg mutation (0 available); any Gars1 mutation (42 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
normal phenotype
• no nervous system phenotype; no axonal degeneration is seen, with large-caliber axons and neuromuscular synapses with normal morphology present and normal nerve conduction velocities




Genotype
MGI:5308220
ht3
Allelic
Composition
Gars1Gt(XM256)6Byg/Gars1C201R
Genetic
Background
involves: 129P2/OlaHsd * BALB/cAnN * C3H/HeH * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gars1C201R mutation (2 available); any Gars1 mutation (42 available)
Gars1Gt(XM256)6Byg mutation (0 available); any Gars1 mutation (42 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• time not specified




Genotype
MGI:3655852
ht4
Allelic
Composition
Gars1Gt(XM256)6Byg/Gars1Nmf249
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gars1Gt(XM256)6Byg mutation (0 available); any Gars1 mutation (42 available)
Gars1Nmf249 mutation (1 available); any Gars1 mutation (42 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging




Genotype
MGI:5308219
cx5
Allelic
Composition
Gars1C201R/Gars1Gt(XM256)6Byg
Tg(CAG-GARS)DRwb/0
Genetic
Background
involves: 129P2/OlaHsd * BALB/cAnN * C3H/HeH * C57BL/6J * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gars1C201R mutation (2 available); any Gars1 mutation (42 available)
Gars1Gt(XM256)6Byg mutation (0 available); any Gars1 mutation (42 available)
Tg(CAG-GARS)DRwb mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
N
• mutants are born at the expected Mendelian ratios, indicating rescue of the embryonic lethality observed in compound heterozygotes without the transgene
• while embryonic lethality is rescued with the transgene, severity of neuropathy is similar to single GarsC201R heterozygotes

growth/size/body
• mutants exhibit lower body weights than single GarsGt(XM256)6Byg heterozygotes or wild-type mice

nervous system
N
• mutants exhibit normal numbers of myelinated axons in the motor or sensory branch of the fremoral nerve
• neuromuscular junctions have regions of immature morphology or denervation, similar to single GarsC201R heterozygotes
• mutants exhibit reduced nerve conduction velocities, but they are similar to single GarsC201R heterozygotes





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last database update
05/07/2024
MGI 6.23
The Jackson Laboratory