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Phenotype ontology term - FYPO:0001766 - abnormal tRNA methylation

Term summary

ID
FYPO:0001766
Name
abnormal tRNA methylation
Ontology or CV name
Phenotype
Definition
A cellular process phenotype observed in the vegetative growth phase of the life cycle in which tRNA methylation, the posttranscriptional addition of methyl groups to specific residues in a tRNA molecule, is abnormal.

Parents

Annotation

Multi-locus phenotype

FYPO:0001768 - abolished tRNA-Asp C38 methylation

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Single locus phenotype

FYPO:0001766 - abnormal tRNA methylation

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FYPO:0007021 - abolished tRNA cytosine 2'-O-methylation

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FYPO:0007022 - abolished tRNA guanosine 2'-O-methylation

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FYPO:0007609 - abolished tRNA guanosine 7-methylation

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FYPO:0003957 - abolished tRNA guanosine N2,N2-dimethylation

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FYPO:0001768 - abolished tRNA-Asp C38 methylation

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FYPO:0007024 - decreased tRNA guanosine 7-methylation

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FYPO:0007025 - decreased tRNA guanosine N2-methylation

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FYPO:0007023 - increased tRNA guanosine 1-methylation

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FYPO:0008129 - increased tRNA guanosine N2,N2-dimethylation

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FYPO:0001769 - increased tRNA-Asp C38 methylation

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