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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Uchl1gad-2J
gracile axonal dystrophy 2 Jackson
MGI:4458326
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Uchl1gad-2J/Uchl1gad-2J B6.Cg-Uchl1gad-2J/GrsrJ MGI:4460998


Genotype
MGI:4460998
hm1
Allelic
Composition
Uchl1gad-2J/Uchl1gad-2J
Genetic
Background
B6.Cg-Uchl1gad-2J/GrsrJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Uchl1gad-2J mutation (1 available); any Uchl1 mutation (29 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging

behavior/neurological
• at 6 or 7 weeks of age the hind legs begin to show weakness characterized by limb grasping, dragging or splaying when walking
• loss of hind limb function progresses to paralysis and premature death

growth/size/body
• a progressive loss in body weight begins at 12 weeks of age

nervous system
• one mouse at 21 weeks of age was assessed and found to have degeneration of long tracks in the spinal cord and extensive neurogenic atrophy in the hind leg





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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
04/16/2024
MGI 6.23
The Jackson Laboratory