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C2 cells depleted of their mitochondrial DNA were fused with synaptosomal fractions from brain tissue of inbred C57BL/6J mice. One clone possessed a 4696bp deletion that spanned from mt-Tk to mt-Nd5 and encompassed 6 tRNA genes and 7 structural genes. This deletion arose spontaneously and does not have direct repeats surrounding the breakpoint. This allele is maintained within cells that contain 30% mutant mitochondria. (J:65025)
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Gene Expression
Related Disease
Reference
Phenotypes
Legend：
hm: homozygous
ht: heterozygous
cn: conditional genotype
cx: complex: > 1 genome feature
tg: involves transgenes
ot: other: hemizygous, indeterminate,...
(F): Female
(M): Male
phenotype observed
N: normal phenotype
(#): related diseases count
Phenotypes：
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| Phenotypes |
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References Literature
Title
PMID
Journal
Year
IF
