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A spontaneous mutation in Polgtm1.1Lrsn mice produced a C to T point mutation at position 5024 (C5024T). This mutation disrupts the same base pair in the acceptor stem as the pathogenic mutation in human with a mitochondrial disease syndrome. (J:238994)
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
