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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(Eno2-ATN1)14Tx
transgene insertion 14, Tian Xu
MGI:4360673
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cx1
Tg(Eno2-ATN1)14Tx/0
Tg(Eno2-ATN1)1Tx/0
FVB.Cg-Tg(Eno2-ATN1)1Tx Tg(Eno2-ATN1)14Tx MGI:4360694
tg2
Tg(Eno2-ATN1)14Tx/0 B6.Cg-Tg(Eno2-ATN1)14Tx MGI:4360692


Genotype
MGI:4360694
cx1
Allelic
Composition
Tg(Eno2-ATN1)14Tx/0
Tg(Eno2-ATN1)1Tx/0
Genetic
Background
FVB.Cg-Tg(Eno2-ATN1)1Tx Tg(Eno2-ATN1)14Tx
Find Mice Using the International Mouse Strain Resource (IMSR)
No mouse lines available in IMSR.
See publication links below for author information.
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• reduced life span

behavior/neurological
• progressively lose the capability to coordinate and balance in the rotarod test and the hanging wire test




Genotype
MGI:4360692
tg2
Allelic
Composition
Tg(Eno2-ATN1)14Tx/0
Genetic
Background
B6.Cg-Tg(Eno2-ATN1)14Tx
Find Mice Using the International Mouse Strain Resource (IMSR)
No mouse lines available in IMSR.
See publication links below for author information.
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• reduced life span
• early-onset Sodium Butyrate (SB, a HDAC inhibitor) treatment (from 4 weeks old) extends their average life span (13.7%)
• late-onset (from 12 weeks old) SB treatment extends the average life span (21.5%)

nervous system
• neurons in the dentate cerebellar nucleus display somal atrophy
• extensive nuclear accumulation of Atrophin-1 and widespread nuclear inclusions in several brain regions (striatum, cortex, thalamus, red nucleus, dentate cerebellar nucleus, and Purkinje cells)

behavior/neurological
• progressively lose the capability to coordinate and balance in the rotarod test and the hanging wire test
• early-onset Sodium Butyrate (SB, a HDAC inhibitor) treatment (from 4 weeks old) delays the onset of motor impairments

reproductive system

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
dentatorubral-pallidoluysian atrophy DOID:0060162 OMIM:125370
J:112706





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last database update
10/29/2024
MGI 6.24
The Jackson Laboratory