About   Help   FAQ
Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Clcn6tm1Tjj
targeted mutation 1, Thomas J Jentsch
MGI:3687967
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Clcn6tm1Tjj/Clcn6tm1Tjj involves: 129S1/Sv * 129X1/SvJ MGI:3688436


Genotype
MGI:3688436
hm1
Allelic
Composition
Clcn6tm1Tjj/Clcn6tm1Tjj
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Clcn6tm1Tjj mutation (0 available); any Clcn6 mutation (89 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Characterization of storage material and axonal swelling in Clcn6tm1Tjj/Clcn6tm1Tjj mice

cellular
• starting at 4 weeks and becoming strong at >3 months in the cortex, autofluorescence of neurons in virtually all brain regions is detected, resulting from lipofuscin accumulation in initial axon segments of neurons; accumulation increases with age

behavior/neurological
• mutants spend less time spent in center of elevated plus maze and number of open-arm entries is reduced in mutants
• mice spend more time in center of test arena, indicating decrease in anxiety
• mutants spend less time in vertical exploratory behavior, as measured by decreased vertical rearings
• mutants show doubled tail-flick latencies compared to wild-type

nervous system
• neurons in the brain show autofluorescence resulting from accumulation of lipofuscin
• soma of cortical neurons show reduced cathepsin D which is concentrated in proximal axons instead; other lysosomal markers are mislocalized in mutants vs wild-type
• cortical neurons frequently show enlargements of the proximal axons, due to lipopigment deposits; deposits consist of lipid droplets associated with amorphous or granular material
• DRG axons have abundant storage material including curvilinear storage bodies and fingerprints
• granular osmophilic deposits (GRODs) in proximal axons contain mitochondrial ATP synthase and lysosomal proteins

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
neuronal ceroid lipofuscinosis 3 DOID:0110731 OMIM:204200
J:113752





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
11/12/2024
MGI 6.24
The Jackson Laboratory