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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Prxtm1Brp
targeted mutation 1, Peter Brophy
MGI:2450150
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Prxtm1Brp/Prxtm1Brp involves: 129P2/Ola * C57BL/6 MGI:3513395
hm2
Prxtm1Brp/Prxtm1Brp involves: 129P2/OlaHsd MGI:5509302
cx3
Prxtm1Brp/Prxtm1Brp
Tg(Mpz/GJB1-Prx*)#Brp/0
involves: 129P2/OlaHsd * C57BL/6 MGI:5431975


Genotype
MGI:3513395
hm1
Allelic
Composition
Prxtm1Brp/Prxtm1Brp
Genetic
Background
involves: 129P2/Ola * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Prxtm1Brp mutation (0 available); any Prx mutation (45 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• inability to eat leading to rapid weight loss
• hindlimb clasping when lifted by the tail is seen between the ages of 4 and 6 weeks with slight tremors as well in some animals
• unsteady gait by 6-9 months of age
• difficulty supporting themselves on their hind limbs
• lower threshold for response using von Frey hairs on hind paws
• lower thermal nociceptive thresholds

growth/size/body
• rapid weight loss due to inability to eat

respiratory system
• labored breathing

nervous system
• growth rate of schwann cells is lower than the extension rate of their axons
• at 6 weeks of age, sciatic nerves display focal thickening and infoldings of internodal myelin
• demyelination
• by 6 months of age, extensive demyelination has occurred in sensory, motor, and autonomic nerves with focal thickening in internodes and axonal sheath disruption
• unmyelinated C fiber bundles are morphologically normal
• remyelination after injury is retarded even in younger mice
• reduced action potentials
• reduced conduction velocity




Genotype
MGI:5509302
hm2
Allelic
Composition
Prxtm1Brp/Prxtm1Brp
Genetic
Background
involves: 129P2/OlaHsd
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Prxtm1Brp mutation (0 available); any Prx mutation (45 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• shorter intermodal lengths
• reduced numbers of Schmidt-Lanterman incisures




Genotype
MGI:5431975
cx3
Allelic
Composition
Prxtm1Brp/Prxtm1Brp
Tg(Mpz/GJB1-Prx*)#Brp/0
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Prxtm1Brp mutation (0 available); any Prx mutation (45 available)
Tg(Mpz/GJB1-Prx*)#Brp mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
N
• intermodal length is normal
• loss of Cajal bands





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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory