About   Help   FAQ
Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Plxna4tm1Hfu
targeted mutation 1, Hajime Fujisawa
MGI:3578655
Summary 4 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Plxna4tm1Hfu/Plxna4tm1Hfu B6.Cg-Plxna4tm1Hfu MGI:3579401
hm2
Plxna4tm1Hfu/Plxna4tm1Hfu involves: C57BL/6 * CBA MGI:3795749
ht3
Plxna4tm1Hfu/Plxna4+ B6.Cg-Plxna4tm1Hfu MGI:3579402
cx4
Plxna2tm1Hfu/Plxna2tm1Hfu
Plxna4tm1Hfu/Plxna4tm1Hfu
involves: C57BL/6 * CBA MGI:3795750


Genotype
MGI:3579401
hm1
Allelic
Composition
Plxna4tm1Hfu/Plxna4tm1Hfu
Genetic
Background
B6.Cg-Plxna4tm1Hfu
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Plxna4tm1Hfu mutation (1 available); any Plxna4 mutation (99 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• trajectories of the cranial and spinal nerves and projections of sympathetic ganglion axons were abnormal, however the position and configuration of cranial and spinal ganglia were normal
• defective pathfinding of fibers from the anterior olfactory nucleus to the anterior commissure
• growth cone collapse of dorsal root ganglion and sympathetic ganglion axons in response to Sema3A, but not Sema3F, was partially reduced and was completely abolished in sympathetic ganglion axons in response to Sema6A
• aberrant projection of sympathetic ganglion axons at E12.5 and E15.5, with axons invading the anterior vertebrate muscles located just medial to sympathetic ganglia and connective tissues surrounding the vertebrae
• both acA (pars anterior) and acP (pars posterior) tracts were absent in the anterior commissure due to defective pathfinding of axons (fibers from the anterior olfactory nucleus never ran dorsally but shifted ventrally and then turned medially at the ventral surface of the forebrain and thus did not end up in the commissure)
• the boundary of each barrel was indistinct, indicating defective formation of the barrels
• defective trajectory and projection of peripheral sensory axons
• distal parts of the facial nerve were disarrayed
• distal parts of the glossopharyngeal nerve were disarrayed
• distal parts of the maxillary and mandibular nerves were disarrayed
• ophthalmic nerve fibers overshot and fanned out in their peripheral target fields
• distal parts of the vagus nerve were disarrayed
• pathways and projections of the spinal nerves were disorganized
• spinal nerve fibers within developing limbs were partially disarrayed and sometimes overshot

cellular
• trajectories of the cranial and spinal nerves and projections of sympathetic ganglion axons were abnormal, however the position and configuration of cranial and spinal ganglia were normal
• defective pathfinding of fibers from the anterior olfactory nucleus to the anterior commissure
• growth cone collapse of dorsal root ganglion and sympathetic ganglion axons in response to Sema3A, but not Sema3F, was partially reduced and was completely abolished in sympathetic ganglion axons in response to Sema6A




Genotype
MGI:3795749
hm2
Allelic
Composition
Plxna4tm1Hfu/Plxna4tm1Hfu
Genetic
Background
involves: C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Plxna4tm1Hfu mutation (1 available); any Plxna4 mutation (99 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• exposure to recombinant SEMA6A protein fails to induce growth cone collapse of mossy fibers from cultured dentate gyrus fragments
• mossy fibers invade most parts of CA3, particularly the stratum lacunosum-moleculare and the stratum oriens (J:135421)
• some fibers enter the suprapyramidal region (normal target) but are not as tightly packed as in wild-type mice (J:135421)
• in slice cocultures mossy fibers from the dentate gyrus massively invade the stratum lacunosum-moleculare and the stratum oriens and diffusely invade the stratum radiatum of either homozygous mutant or wild-type CA3 slices (J:135421)
• mossy fibers aberrantly spread into the stratum radiatum, stratum oriens, and stratum lacunosum-moleculare compared to in wild-type mice (J:160509)
• mossy fibers invade the inner and outer molecular layer of the dentate gyrus unlike in wild-type mice (J:160509)

cellular
• exposure to recombinant SEMA6A protein fails to induce growth cone collapse of mossy fibers from cultured dentate gyrus fragments




Genotype
MGI:3579402
ht3
Allelic
Composition
Plxna4tm1Hfu/Plxna4+
Genetic
Background
B6.Cg-Plxna4tm1Hfu
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Plxna4tm1Hfu mutation (1 available); any Plxna4 mutation (99 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• growth cone collapse of dorsal root ganglion and sympathetic ganglion axons in response to Sema3A, but not Sema3F, and sympathetic ganglion axons in response to Sema6A was partially reduced
• thin acA (pars anterior) tract
• extremely thin or missing acP (pars posterior) tract
• abnormal trajectories and projections of the cranial nerves that were less severe than in homozygotes
• abnormal trajectories and projections of the spinal nerves that were less severe than in homozgyotes

cellular
• growth cone collapse of dorsal root ganglion and sympathetic ganglion axons in response to Sema3A, but not Sema3F, and sympathetic ganglion axons in response to Sema6A was partially reduced




Genotype
MGI:3795750
cx4
Allelic
Composition
Plxna2tm1Hfu/Plxna2tm1Hfu
Plxna4tm1Hfu/Plxna4tm1Hfu
Genetic
Background
involves: C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Plxna2tm1Hfu mutation (1 available); any Plxna2 mutation (127 available)
Plxna4tm1Hfu mutation (1 available); any Plxna4 mutation (99 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• mossy fibers are widely distributed in CA3 as in mice homozygous for Plxna4tm1Hfu alone





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
04/30/2024
MGI 6.23
The Jackson Laboratory