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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Oxr1tm1a(EUCOMM)Wtsi
targeted mutation 1a, Wellcome Trust Sanger Institute
MGI:4461745
Summary 4 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Oxr1tm1a(EUCOMM)Wtsi/Oxr1tm1a(EUCOMM)Wtsi C57BL/6N-Oxr1tm1a(EUCOMM)Wtsi MGI:5796653
ht2
Oxr1tm1a(EUCOMM)Wtsi/Oxr1+ C57BL/6N-Oxr1tm1a(EUCOMM)Wtsi/Wtsi MGI:6461506
cx3
Ncoa7em1Pelo/Ncoa7+
Oxr1tm1a(EUCOMM)Wtsi/Oxr1tm1a(EUCOMM)Wtsi
involves: C57BL/6J * C57BL/6N MGI:6714042
cx4
Ncoa7em1Pelo/Ncoa7em1Pelo
Oxr1tm1a(EUCOMM)Wtsi/Oxr1tm1a(EUCOMM)Wtsi
involves: C57BL/6J * C57BL/6N MGI:6714043


Genotype
MGI:5796653
hm1
Allelic
Composition
Oxr1tm1a(EUCOMM)Wtsi/Oxr1tm1a(EUCOMM)Wtsi
Genetic
Background
C57BL/6N-Oxr1tm1a(EUCOMM)Wtsi
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Oxr1tm1a(EUCOMM)Wtsi mutation (1 available); any Oxr1 mutation (37 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Oxr1tm1a(EUCOMM)Wtsi/Oxr1tm1a(EUCOMM)Wtsi and bella/bella mice show increased apoptosis in the granule cell layer of the cerebellum

mortality/aging

behavior/neurological
• homozygotes display ataxia to the same extent and over an identical time course as bella homozygotes

nervous system
• at P21, homozygotes show a significant increase in TUNEL-positive cells in the granule cell layer of the cerebellum with a pattern and distribution equivalent to that seen in bella homozygotes
• homozygotes display progressive cerebellar degeneration to the same extent and over an identical time course as bella homozygotes

cellular
• at P21, homozygotes show a significant increase in TUNEL-positive cells in the granule cell layer of the cerebellum with a pattern and distribution equivalent to that seen in bella homozygotes




Genotype
MGI:6461506
ht2
Allelic
Composition
Oxr1tm1a(EUCOMM)Wtsi/Oxr1+
Genetic
Background
C57BL/6N-Oxr1tm1a(EUCOMM)Wtsi/Wtsi
Cell Lines EPD0600_1_B09
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Oxr1tm1a(EUCOMM)Wtsi mutation (1 available); any Oxr1 mutation (37 available)
Data Sources
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body

hematopoietic system
IMPC - WTSI




Genotype
MGI:6714042
cx3
Allelic
Composition
Ncoa7em1Pelo/Ncoa7+
Oxr1tm1a(EUCOMM)Wtsi/Oxr1tm1a(EUCOMM)Wtsi
Genetic
Background
involves: C57BL/6J * C57BL/6N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ncoa7em1Pelo mutation (0 available); any Ncoa7 mutation (199 available)
Oxr1tm1a(EUCOMM)Wtsi mutation (1 available); any Oxr1 mutation (37 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• early-onset




Genotype
MGI:6714043
cx4
Allelic
Composition
Ncoa7em1Pelo/Ncoa7em1Pelo
Oxr1tm1a(EUCOMM)Wtsi/Oxr1tm1a(EUCOMM)Wtsi
Genetic
Background
involves: C57BL/6J * C57BL/6N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ncoa7em1Pelo mutation (0 available); any Ncoa7 mutation (199 available)
Oxr1tm1a(EUCOMM)Wtsi mutation (1 available); any Oxr1 mutation (37 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging





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last database update
10/09/2024
MGI 6.24
The Jackson Laboratory