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Phenotype ontology term - FYPO:0000189 - abnormal mRNA splicing, via spliceosome

Term summary

ID
FYPO:0000189
Name
abnormal mRNA splicing, via spliceosome
Ontology or CV name
Phenotype
Definition
A cellular process phenotype in which mRNA splicing via the spliceosome is abnormal.

Parents

Annotation

Multi-locus phenotype

FYPO:0003602 - abolished mRNA splicing, via spliceosome

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FYPO:0003029 - decreased mRNA splicing, via spliceosome

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FYPO:0003244 - decreased mRNA splicing, via spliceosome, intron-specific

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FYPO:0008118 - decreased splicing of introns with branch point-distant 3’-splice site

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FYPO:0008113 - increased intron retention

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Single locus phenotype

FYPO:0000189 - abnormal mRNA splicing, via spliceosome

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FYPO:0003602 - abolished mRNA splicing, via spliceosome

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FYPO:0008147 - decreased mRNA splicing, meiotic genes

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FYPO:0003029 - decreased mRNA splicing, via spliceosome

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FYPO:0003244 - decreased mRNA splicing, via spliceosome, intron-specific

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FYPO:0008118 - decreased splicing of introns with branch point-distant 3’-splice site

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FYPO:0003242 - decreased splicing of mRNA introns with low A/U content

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FYPO:0003030 - decreased splicing of mRNA introns with low A/U content and polypyrimidine tracts distal to branch site

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FYPO:0007199 - decreased splicing of mRNA introns with nonconsensus cis-splicing sequences

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FYPO:0008113 - increased intron retention

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FYPO:0003470 - increased mRNA splicing, via spliceosome

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