Phenotype ontology term - FYPO:0003973 - abnormal nuclear pore localization

Term summary

ID: FYPO:0003973
Name: abnormal nuclear pore localization
Ontology or CV name: Phenotype
Definition: A localization phenotype observed in the vegetative growth phase of the life cycle in which nuclear pore localization is abnormal, resulting in an abnormal spatial arrangement of nuclear pores within the nuclear envelope.

Parents

is_a abnormal cellular process during vegetative growth

Annotation

Multi-locus phenotype

FYPO:0003783 - abnormal nuclear pore localization during mitosis

References:

PMID:32848252

Genes:

Genotypes:

imp1delta les1delta

Single locus phenotype

FYPO:0003973 - abnormal nuclear pore localization

References:

PMID:28242692

Genes:

vps4 (SPAC2G11.06)

Genotypes:

vps4delta

FYPO:0003783 - abnormal nuclear pore localization during mitosis

References:

Genes:

Genotypes:

FYPO:0007547 - abnormal nuclear pore localization to mitotic nuclear bridge midzone membrane

References:

Genes:

Genotypes:

FYPO:0010034 - abolished nuclear pore clustering during cellular response to hydroxyurea

References:

PMID:41259369

Genes:

Genotypes:

FYPO:0007458 - abolished nuclear pore localization to mitotic nuclear bridge

References:

PMID:32848252

Genes:

les1 (SPAC23C4.05c)

Genotypes:

les1delta

FYPO:0003978 - inviable vegetative cell with fragmented nuclear envelope and nuclear pore aggregation in cytoplasm during mitotic telophase

References:

PMID:7877997

Genes:

pim1 (SPBC557.03c)

Genotypes:

pim1-d1(unknown)