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Phenotype ontology term - FYPO:0000169 - abnormal chromatin silencing at subtelomere

Term summary

ID
FYPO:0000169
Name
abnormal chromatin silencing at subtelomere
Ontology or CV name
Phenotype
Definition
A transcription regulation phenotype observed in the vegetative growth phase of the life cycle in which chromatin silencing at subtelomeric regions is abnormal. Chromatin silencing is the observed effect of processes that repress transcription in a region of the genome that is normally assembled into heterochromatin.

Parents

Annotation

Multi-locus phenotype

FYPO:0004604 - decreased chromatin silencing at subtelomere

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FYPO:0004542 - increased chromatin silencing at subtelomere

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Single locus phenotype

FYPO:0000169 - abnormal chromatin silencing at subtelomere

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Genotypes:

FYPO:0004604 - decreased chromatin silencing at subtelomere

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Genotypes:

FYPO:0004542 - increased chromatin silencing at subtelomere

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Genes:

Genotypes: