About   Help   FAQ
Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Plxna3tm1Matl
targeted mutation 1, Marc Tessier-Lavigne
MGI:2386961
Summary 6 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Plxna3tm1Matl/Plxna3tm1Matl either: (involves: 129S1/Sv * C57BL/6) or (involves: 129S1/Sv * CD-1) MGI:3041539
hm2
Plxna3tm1Matl/Plxna3tm1Matl involves: 129S1/Sv MGI:5007635
cx3
Plxna3tm1Matl/Y
Plxna4tm1Matl/Plxna4tm1Matl
either: (involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6) or (involves: 129P2/OlaHsd * 129S1/Sv * CD-1) MGI:3579482
cx4
Plxna3tm1Matl/Plxna3tm1Matl
Plxna4tm1Matl/Plxna4tm1Matl
either: (involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6) or (involves: 129P2/OlaHsd * 129S1/Sv * CD-1) MGI:3590677
cx5
Plxna1tm1Tmj/Plxna1tm1Tmj
Plxna3tm1Matl/Plxna3tm1Matl
involves: 129S/SvEv * 129S1/Sv MGI:5284893
ot6
Plxna3tm1Matl/Y either: (involves: 129S1/Sv * C57BL/6) or (involves: 129S1/Sv * CD-1) MGI:3041540


Genotype
MGI:3041539
hm1
Allelic
Composition
Plxna3tm1Matl/Plxna3tm1Matl
Genetic
Background
either: (involves: 129S1/Sv * C57BL/6) or (involves: 129S1/Sv * CD-1)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Plxna3tm1Matl mutation (1 available); any Plxna3 mutation (13 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• repulsive effect of Sema3A and Sema3F on axon growth from sympathetic nerves, dorsal root ganglia and areas of the hippocampus is eliminated
• axon pruning directed by Sema3A does not occur
• afferent pathways from CA3 to the contralateral hippocampus is underdeveloped
• the few axons entering the contralateral hippocampus terminate inappropriately
• most axons are misrouted ipsilaterally
• infrapyramidal bundle fails to rejoin the main mossy fiber pathway (J:72426)
• infrapyramidal bundle fails to shorten as it does in wild-type mice (J:83314)
• ophthalmic branch defasciculated at E10.5 through E11.5
• cranial nerve projections normal at E10.5

cellular
• repulsive effect of Sema3A and Sema3F on axon growth from sympathetic nerves, dorsal root ganglia and areas of the hippocampus is eliminated
• axon pruning directed by Sema3A does not occur




Genotype
MGI:5007635
hm2
Allelic
Composition
Plxna3tm1Matl/Plxna3tm1Matl
Genetic
Background
involves: 129S1/Sv
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Plxna3tm1Matl mutation (1 available); any Plxna3 mutation (13 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
N
• mice exhibit normal retinal stratification




Genotype
MGI:3579482
cx3
Allelic
Composition
Plxna3tm1Matl/Y
Plxna4tm1Matl/Plxna4tm1Matl
Genetic
Background
either: (involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6) or (involves: 129P2/OlaHsd * 129S1/Sv * CD-1)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Plxna3tm1Matl mutation (1 available); any Plxna3 mutation (13 available)
Plxna4tm1Matl mutation (2 available); any Plxna4 mutation (99 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• repulsive effect of Sema3A on axon growth from sensory neurons of the dorsal root ganglia and of superior cervical ganglion neurons was eliminated
• starting at E11.5, had severely disrupted peripheral sensory projections, with many axons crossing the dorsal midline to the other side of the body at E12.5
• peripheral sensory projections exhibited extensive outgrowth and branching as if there were no boundaries for the axons
• severely disorganized and derasciculated ophthalmic, maxillary and mandibular projections at E11.5
• more fibers of the ophthalmic branch misprojected in different directions, and some even started to invade the eye region at E11.5 and the ophthalmic axon fibers covered the entire face, including the eyes and the fibers were thinner and heavily branched at E12.5 compared to wildtype
• severely defasciculated even though individual axons could still be seen leaving the midbrain-hindbrain junction

cellular
• repulsive effect of Sema3A on axon growth from sensory neurons of the dorsal root ganglia and of superior cervical ganglion neurons was eliminated




Genotype
MGI:3590677
cx4
Allelic
Composition
Plxna3tm1Matl/Plxna3tm1Matl
Plxna4tm1Matl/Plxna4tm1Matl
Genetic
Background
either: (involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6) or (involves: 129P2/OlaHsd * 129S1/Sv * CD-1)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Plxna3tm1Matl mutation (1 available); any Plxna3 mutation (13 available)
Plxna4tm1Matl mutation (2 available); any Plxna4 mutation (99 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• repulsive effect of Sema3A on axon growth from sensory neurons of the dorsal root ganglia and of superior cervical ganglion neurons was eliminated
• starting at E11.5, had severely disrupted peripheral sensory projections, with many axons crossing the dorsal midline to the other side of the body at E12.5
• peripheral sensory projections exhibited extensive outgrowth and branching as if there were no boundaries for the axons
• severely disorganized and derasciculated ophthalmic, maxillary and mandibular projections at E11.5
• more fibers of the ophthalmic branch misprojected in different directions, and some even started to invade the eye region at E11.5 and the ophthalmic axon fibers covered the entire face, including the eyes and the fibers were thinner and heavily branched at E12.5 compared to wildtype
• severely defasciculated even though individual axons could still be seen leaving the midbrain-hindbrain junction

cellular
• repulsive effect of Sema3A on axon growth from sensory neurons of the dorsal root ganglia and of superior cervical ganglion neurons was eliminated




Genotype
MGI:5284893
cx5
Allelic
Composition
Plxna1tm1Tmj/Plxna1tm1Tmj
Plxna3tm1Matl/Plxna3tm1Matl
Genetic
Background
involves: 129S/SvEv * 129S1/Sv
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Plxna1tm1Tmj mutation (0 available); any Plxna1 mutation (75 available)
Plxna3tm1Matl mutation (1 available); any Plxna3 mutation (13 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
• multiple amacrine cell subtypes exhibit aberrant neurite extension into the inner nuclear layer and outer plexiform layer
• multiple retinal bipolar cell subtypes exhibit aberrant neurite extension into the inner nuclear layer and outer plexiform layer
• multiple retinal ganglion subtypes exhibit aberrant neurite extension into the inner nuclear layer and outer plexiform layer
• multiple retinal ganglion, amacrine and bipolar cell subtypes exhibit aberrant neurite extension into the inner nuclear layer and outer plexiform layer
• exhibit severe, fully penetrant and expressive, defects in inner plexiform layer neurite targeting
• multiple retinal ganglion, amacrine and bipolar cell subtypes exhibit aberrant neurite extension into the inner nuclear layer and outer plexiform layer

nervous system
• exhibit severe, fully penetrant and expressive, defects in inner plexiform layer neurite targeting
• multiple retinal ganglion, amacrine and bipolar cell subtypes exhibit aberrant neurite extension into the inner nuclear layer and outer plexiform layer
• multiple amacrine cell subtypes exhibit aberrant neurite extension into the inner nuclear layer and outer plexiform layer
• multiple retinal bipolar cell subtypes exhibit aberrant neurite extension into the inner nuclear layer and outer plexiform layer
• multiple retinal ganglion subtypes exhibit aberrant neurite extension into the inner nuclear layer and outer plexiform layer




Genotype
MGI:3041540
ot6
Allelic
Composition
Plxna3tm1Matl/Y
Genetic
Background
either: (involves: 129S1/Sv * C57BL/6) or (involves: 129S1/Sv * CD-1)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Plxna3tm1Matl mutation (1 available); any Plxna3 mutation (13 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• repulsive effect of Sema3A and Sema3F on axon growth from sympathetic nerves, dorsal root ganglia and areas of the hippocampus is eliminated
• axon pruning directed by Sema3A does not occur
• afferent pathways from CA3 to the contralateral hippocampus is underdeveloped
• the few axons entering the contralateral hippocampus terminate inappropriately
• most axons are misrouted ipsilaterally
• infrapyramidal bundle fails to rejoin the main mossy fiber pathway (J:72426)
• infrapyramidal bundle fails to shorten as it does in wild-type mice (J:83314)
• ophthalmic branch defasciculated at E10.5 through E11.5
• cranial nerve projections normal at E10.5

cellular
• repulsive effect of Sema3A and Sema3F on axon growth from sympathetic nerves, dorsal root ganglia and areas of the hippocampus is eliminated
• axon pruning directed by Sema3A does not occur





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
11/19/2024
MGI 6.24
The Jackson Laboratory