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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Nudt1tm1Tts
targeted mutation 1, Teruhisa Tsuzuki
MGI:2387695
Summary 7 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Nudt1tm1Tts/Nudt1tm1Tts B6.129S-Nudt1tm1Tts MGI:3784585
hm2
Nudt1tm1Tts/Nudt1tm1Tts involves: 129S/SvEv * C57BL/6 * DBA/2 MGI:3055984
hm3
Nudt1tm1Tts/Nudt1tm1Tts involves: 129S/SvEv * C57BL/6JJcl MGI:5476989
cx4
Mutyhtm1Yun/Mutyhtm1Yun
Nudt1tm1Tts/Nudt1tm1Tts
Ogg1tm1Yun/Ogg1tm1Yun
B6JJcl.129-Mutyhtm1Yun Nudt1tm1Tts Ogg1tm1Yun MGI:5476986
cx5
Nudt1tm1Tts/Nudt1tm1Tts
Ogg1tm1Yun/Ogg1tm1Yun
involves: 129S/SvEv * C57BL/6J MGI:2653017
cx6
Msh2tm1Tts/Msh2tm1Tts
Nudt1tm1Tts/Nudt1tm1Tts
involves: 129S/SvEv * C57BL/6J MGI:3784584
cx7
Nudt1tm1Tts/Nudt1tm1Tts
Ogg1tm1Yun/Ogg1tm1Yun
involves: 129S/SvEv * C57BL/6JJcl MGI:5476988


Genotype
MGI:3784585
hm1
Allelic
Composition
Nudt1tm1Tts/Nudt1tm1Tts
Genetic
Background
B6.129S-Nudt1tm1Tts
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nudt1tm1Tts mutation (0 available); any Nudt1 mutation (31 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
• G:C->A:T transversions are increased in frequency compared to Nudt-null mice




Genotype
MGI:3055984
hm2
Allelic
Composition
Nudt1tm1Tts/Nudt1tm1Tts
Genetic
Background
involves: 129S/SvEv * C57BL/6 * DBA/2
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nudt1tm1Tts mutation (0 available); any Nudt1 mutation (31 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
neoplasm
• lesions of the glandular stomach are 3 times as frequent as in controls
• adenomatous hyperplasia, adenomas, and adenocarcinoma
• liver tumors in 38% of males as opposed to 13% of control males
• liver tumors in 3.9% of females as opposed to none in female controls
• found in greater numbers at age 1.5 years
• found in greater numbers at age 1.5 years

digestive/alimentary system
• lesions of the glandular stomach are 3 times as frequent as in controls
• adenomatous hyperplasia, adenomas, and adenocarcinoma

respiratory system
• found in greater numbers at age 1.5 years
• found in greater numbers at age 1.5 years

liver/biliary system
• liver tumors in 38% of males as opposed to 13% of control males
• liver tumors in 3.9% of females as opposed to none in female controls




Genotype
MGI:5476989
hm3
Allelic
Composition
Nudt1tm1Tts/Nudt1tm1Tts
Genetic
Background
involves: 129S/SvEv * C57BL/6JJcl
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nudt1tm1Tts mutation (0 available); any Nudt1 mutation (31 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
N
• 3-NP-treated mice exhibit normal distance traveled in an open-field test




Genotype
MGI:5476986
cx4
Allelic
Composition
Mutyhtm1Yun/Mutyhtm1Yun
Nudt1tm1Tts/Nudt1tm1Tts
Ogg1tm1Yun/Ogg1tm1Yun
Genetic
Background
B6JJcl.129-Mutyhtm1Yun Nudt1tm1Tts Ogg1tm1Yun
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mutyhtm1Yun mutation (2 available); any Mutyh mutation (36 available)
Nudt1tm1Tts mutation (0 available); any Nudt1 mutation (31 available)
Ogg1tm1Yun mutation (1 available); any Ogg1 mutation (23 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
neoplasm
• mice are highly susceptible to spontaneous tumorigenesis within 100 days of birth




Genotype
MGI:2653017
cx5
Allelic
Composition
Nudt1tm1Tts/Nudt1tm1Tts
Ogg1tm1Yun/Ogg1tm1Yun
Genetic
Background
involves: 129S/SvEv * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nudt1tm1Tts mutation (0 available); any Nudt1 mutation (31 available)
Ogg1tm1Yun mutation (1 available); any Ogg1 mutation (23 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
neoplasm
N
• no tumors in the lungs of double knockout mice, unlike Oggtm1Skmi single knockout mice




Genotype
MGI:3784584
cx6
Allelic
Composition
Msh2tm1Tts/Msh2tm1Tts
Nudt1tm1Tts/Nudt1tm1Tts
Genetic
Background
involves: 129S/SvEv * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Msh2tm1Tts mutation (0 available); any Msh2 mutation (95 available)
Nudt1tm1Tts mutation (0 available); any Nudt1 mutation (31 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
• spleen cells show a significant increase in frameshift mutations at mononucleotide runs relative to wild-type when assayed with a reporter system




Genotype
MGI:5476988
cx7
Allelic
Composition
Nudt1tm1Tts/Nudt1tm1Tts
Ogg1tm1Yun/Ogg1tm1Yun
Genetic
Background
involves: 129S/SvEv * C57BL/6JJcl
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nudt1tm1Tts mutation (0 available); any Nudt1 mutation (31 available)
Ogg1tm1Yun mutation (1 available); any Ogg1 mutation (23 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• striatal degeneration in 3-NP-treated mice
• however, calpain and PARP inhibitors suppress striatal neurodegeneration and behavioral impairments
• in 3-NP-treated mice, especially in the dorsal striatum
• striatal degeneration in 3-NP-treated mice
• however, calpain and PARP inhibitors suppress striatal neurodegeneration and behavioral impairments

behavior/neurological
• 3-NP treated mice exhibit increased motor impairment (neurological score based on: general slowness of displacement resulting from mild hindlimb impairment;, incoordination and marked gait abnormality; hindlimb paralysis; incapacity to move resulting from forelimb and hindlimb impairment) compared with wild-type mice
• in 3-NP-treated mice
• 3-NP-treated mice travel less distance in an open-field test compared with wild-type mice that is more severe than in Ogg1tm1Skmi homozygotes
• 3-NP-treated mice are hypoactive in home cages compared with wild-type mice
• however, calpain and PARP inhibitors suppress striatal neurodegeneration and behavioral impairments

cellular
• striatal degeneration in 3-NP-treated mice
• however, calpain and PARP inhibitors suppress striatal neurodegeneration and behavioral impairments
• 3-NP treated mice exhibit an accumulation of 8-oxoG that results in the accumulation of single strand breaks in mitochondrial DNA of striatal medium spiny neurons and nuclear DNA of striatal microglia compared with wild-type mice

homeostasis/metabolism
• striatal degeneration in 3-NP-treated mice
• however, calpain and PARP inhibitors suppress striatal neurodegeneration and behavioral impairments
• 3-NP treated mice exhibit an accumulation of 8-oxoG that results in the accumulation of single strand breaks in mitochondrial DNA of striatal medium spiny neurons and nuclear DNA of striatal microglia compared with wild-type mice

immune system
• in 3-NP-treated mice, especially in the dorsal striatum

hematopoietic system
• in 3-NP-treated mice, especially in the dorsal striatum





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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory