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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(tetO/CMV-Pmp22)JP18Clh
transgene insertion JP18, Clare Huxley
MGI:5779548
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
cx1
Tg(PMP22-tTA)JY13Clh/0
Tg(tetO/CMV-Pmp22)JP18Clh/0
involves: C57BL/6J * CBA/Ca MGI:5779551


Genotype
MGI:5779551
cx1
Allelic
Composition
Tg(PMP22-tTA)JY13Clh/0
Tg(tetO/CMV-Pmp22)JP18Clh/0
Genetic
Background
involves: C57BL/6J * CBA/Ca
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tg(PMP22-tTA)JY13Clh mutation (0 available)
Tg(tetO/CMV-Pmp22)JP18Clh mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• slightly abnormal gait

nervous system
• 26% of axons within the sciatic nerve exhibit very thin or absent myelin
• mice fed tetracycline at 8 weeks of age to turn off transgene expression show myelination of non-myelinated fibers within 1 week of tetracycline feeding, however myelin sheaths of these fibers are still very thin by 2 weeks of feeding
• mice fed tetracycline at 8 weeks of age for 4-12 weeks show a dramatic decrease in the percentage of very thinly myelinated fibers, however the myelin sill has not reached normal thickness
• a proportion of axons in 16 week old mice (particularly medium and smaller sized axons) have very thin or no myelin
• mice administered tetracycline from at least a week before birth to turn off transgene expression exhibit nearly normal myelin thickness at 16 weeks of age and only about 1% of axons show very thin or absent myelin
• mice fed tetracycline from before birth to 8 weeks of age develop nearly normal mature myelin
• mice fed tetracycline from before birth to 8 weeks of age at which age tetracycline was removed to turn on transgene expression show some demyelination such that after 8 weeks of expression, 9% of fibers are demyelinated
• motor nerve conduction velocity in the sciatic/tibial nerves is slightly reduced

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
Charcot-Marie-Tooth disease type 1A DOID:0110148 OMIM:118220
J:69545





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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
11/19/2024
MGI 6.24
The Jackson Laboratory