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Phenotype ontology term - FYPO:0001765 - abnormal tRNA modification

Term summary

ID
FYPO:0001765
Name
abnormal tRNA modification
Ontology or CV name
Phenotype
Definition
A cellular process phenotype observed in the vegetative growth phase of the life cycle in which tRNA modification, the covalent alteration of one or more nucleotides within 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:0008450 - abnormal tRNA modification at postion A37

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FYPO:0008451 - abnormal tRNA modification at postion A58

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FYPO:0008449 - abnormal tRNA modification at postion U34

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FYPO:0008345 - abolished tRNA cytidine N4-acetylation

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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:0003218 - abolished tRNA wobble base 5-methoxycarbonylmethyl-2-thiouridine biosynthesis

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FYPO:0005177 - abolished tRNA wobble position uridine thiolation

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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:0007026 - decreased tRNA wybutosine biosynthesis

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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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