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Phenotype ontology term - FYPO:0000468 - abnormal mating type switching

Term summary

ID
FYPO:0000468
Name
abnormal mating type switching
Ontology or CV name
Phenotype
Definition
A cellular process phenotype observed in the vegetative growth phase of the life cycle in which mating type switching is abnormal.

Parents

Annotation

Multi-locus phenotype

FYPO:0000468 - abnormal mating type switching

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FYPO:0000469 - abolished mating type switching

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Genotypes:

FYPO:0003081 - decreased genetic imprinting at mating-type locus

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FYPO:0000470 - decreased mating type switching

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Genotypes:

FYPO:0005357 - decreased site-specific DNA replication termination at RTS1 barrier

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Single locus phenotype

FYPO:0000468 - abnormal mating type switching

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Genes:

Genotypes:

FYPO:0003659 - abnormal mating type switching resulting in duplication or deletion in mating-type region

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Genotypes:

FYPO:0003080 - abolished genetic imprinting at mating-type locus

References:

Genes:

Genotypes:

FYPO:0000469 - abolished mating type switching

References:

Genes:

Genotypes:

FYPO:0005356 - abolished site-specific DNA replication termination at RTS1 barrier

References:

Genes:

Genotypes:

FYPO:0003081 - decreased genetic imprinting at mating-type locus

References:

Genes:

Genotypes:

FYPO:0000470 - decreased mating type switching

References:

Genes:

Genotypes:

FYPO:0005357 - decreased site-specific DNA replication termination at RTS1 barrier

References:

Genes:

Genotypes:

FYPO:0000471 - increased mating type switching

References:

Genes:

Genotypes:

FYPO:0005358 - increased site-specific DNA replication termination at RTS1 barrier

References:

Genes:

Genotypes: