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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(Thy1-YFP)16Jrs
transgene insertion 16, Joshua R Sanes
MGI:3505585
Summary 6 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cx1
Nrp1tm1Ddg/Nrp1tm1Ddg
Tg(Thy1-YFP)16Jrs/0
involves: 129P2/OlaHsd * C57BL/6 MGI:3512124
cx2
Fgfbp1tm1Gvdz/Fgfbp1tm1Gvdz
Tg(Thy1-YFP)16Jrs/0
involves: 129S5/SvEvBrd * C57BL/6J * CBA MGI:5902844
cx3
Fgfbp1tm1Gvdz/Fgfbp1tm1Gvdz
Tg(SOD1*G93A)1Gur/0
Tg(Thy1-YFP)16Jrs/0
involves: 129S5/SvEvBrd * C57BL/6J * CBA * SJL MGI:5902841
cx4
Gars1C201R/Gars1+
Tg(Thy1-YFP)16Jrs/?
involves: BALB/cAnN * C3H/HeH * C57BL/6J * CBA MGI:5752648
cx5
Dynlrb1tm1a(EUCOMM)Wtsi/Dynlrb1+
Tg(Thy1-YFP)16Jrs/0
involves: C57BL/6J * C57BL/6N MGI:6466700
cx6
Gars1Nmf249/Gars1+
Tg(Thy1-YFP)16Jrs/?
involves: C57BL/6J * CAST/Ei * CBA/J MGI:5752579


Genotype
MGI:3512124
cx1
Allelic
Composition
Nrp1tm1Ddg/Nrp1tm1Ddg
Tg(Thy1-YFP)16Jrs/0
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nrp1tm1Ddg mutation (2 available); any Nrp1 mutation (81 available)
Tg(Thy1-YFP)16Jrs mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• basal dendrites of layer 5 cortical neurons within the neocortex were markedly diminished in length and complexity




Genotype
MGI:5902844
cx2
Allelic
Composition
Fgfbp1tm1Gvdz/Fgfbp1tm1Gvdz
Tg(Thy1-YFP)16Jrs/0
Genetic
Background
involves: 129S5/SvEvBrd * C57BL/6J * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fgfbp1tm1Gvdz mutation (0 available); any Fgfbp1 mutation (18 available)
Tg(Thy1-YFP)16Jrs mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• increased number of fragmented neuromuscular junctions at 12 months compared with control mice




Genotype
MGI:5902841
cx3
Allelic
Composition
Fgfbp1tm1Gvdz/Fgfbp1tm1Gvdz
Tg(SOD1*G93A)1Gur/0
Tg(Thy1-YFP)16Jrs/0
Genetic
Background
involves: 129S5/SvEvBrd * C57BL/6J * CBA * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fgfbp1tm1Gvdz mutation (0 available); any Fgfbp1 mutation (18 available)
Tg(SOD1*G93A)1Gur mutation (4 available)
Tg(Thy1-YFP)16Jrs mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• accelerated in female and male mice compared with Tg(SOD1*G93A)1Gur mice

nervous system
• fewer fully innervated neuromuscular junctions (NMJs) than in Tg(SOD1*G93A)1Gur mice with more partially and completely denervated NMJs




Genotype
MGI:5752648
cx4
Allelic
Composition
Gars1C201R/Gars1+
Tg(Thy1-YFP)16Jrs/?
Genetic
Background
involves: BALB/cAnN * C3H/HeH * C57BL/6J * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gars1C201R mutation (2 available); any Gars1 mutation (42 available)
Tg(Thy1-YFP)16Jrs mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• at high magnification, but not evident at low magnification, approximately 5% of the neuromuscular junctions assesed in the levator auris longus at 4 months of age are found to be only partially innervated, far fewer than in Nmf249 heterozygotes
• nearly all terminals assessed in the levator auris longus show more diffuse postsynaptic staining, less distinct gutters, thinner axons and presynaptic nerves, synapses that are smaller than in wild-type controls, the average quantal content is significantly lower than normal, and the quantal content and mean evoked endplate currents are lower still at 4 months compared with 2 months
• at 2 months of age 25% decrease in amplitude of evoked endplate currents, and quantal content in neuromuscular synapses of the levator auris longus muscle, and treatment with 3,4-DAP or physostigmine increases the in vivo evoked endplate currents at 4 months of age
• at 2 months of age the frequency of spontaneous release is consistently lower than normal although the quantal amplitude at synapses is normal, and no differences are found in the miniature endplate current amplitude

behavior/neurological
• compared with wild-type controls, heterozygotes have impaired grip strength and this is improved by treatment with physostigmine, but made worse by treatment with 3,4-DAP




Genotype
MGI:6466700
cx5
Allelic
Composition
Dynlrb1tm1a(EUCOMM)Wtsi/Dynlrb1+
Tg(Thy1-YFP)16Jrs/0
Genetic
Background
involves: C57BL/6J * C57BL/6N
Cell Lines EPD0373_7_C01
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dynlrb1tm1a(EUCOMM)Wtsi mutation (1 available); any Dynlrb1 mutation (12 available)
Tg(Thy1-YFP)16Jrs mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• DRG neurons exhibit significantly reduced axon outgrowth after 48 h in culture

cellular
• DRG neurons exhibit significantly reduced axon outgrowth after 48 h in culture




Genotype
MGI:5752579
cx6
Allelic
Composition
Gars1Nmf249/Gars1+
Tg(Thy1-YFP)16Jrs/?
Genetic
Background
involves: C57BL/6J * CAST/Ei * CBA/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gars1Nmf249 mutation (1 available); any Gars1 mutation (42 available)
Tg(Thy1-YFP)16Jrs mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• nearly all terminals assessed in the levator auris longus show more diffuse postsynaptic staining, less distinct gutters, thinner axons and presynaptic nerves, synapses that are smaller than in wild-type controls, fewer mitochondria at the synaptic terminals, and the average quantal content is significantly lower than normal
• at high magnification, but not evident at low magnification, approximately half of the junctions assesed in the levator auris longus at 2 months of age are found to be only partially innervated, even in the mildly affected mice, and there are more than 3 times as many denervated junctions at 2 months of age as are found in carriers of the C201R allele at 4 months of age
• at 2 months of age 25% decrease in amplitude of evoked endplate currents, and quantal content in neuromuscular synapses the levator auris longus muscle
• at 2 months of age the frequency of spontaneous release is consistently lower than normal although the quantal amplitude at synapses is normal, and no differences are found in the miniature endplate current amplitude

behavior/neurological
• compared with wild-type controls, heterozygotes have impaired grip strength and this is improved by treatment with physostigmine





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