Phenotype ontology term - FYPO:0006057 - abnormal vacuole fusion

Term summary

ID: FYPO:0006057
Name: abnormal vacuole fusion
Ontology or CV name: Phenotype
Definition: A cellular process phenotype in which vacuole fusion, the merging of two vacuole membranes to form a single vacuole, is abnormal.

Parents

is_a abnormal cellular process

Annotation

Multi-locus phenotype

FYPO:0004483 - abnormal vacuole fusion during cellular hypotonic response

References:

PMID:20388730

Genes:

Genotypes:

imt1delta imt2delta imt3delta

FYPO:0004482 - abnormal vacuole fusion during vegetative growth

References:

PMID:22344254

Genes:

Genotypes:

gtr1-Q61L(aa) vam6delta

Single locus phenotype

FYPO:0006057 - abnormal vacuole fusion

References:

PMID:19643199

Genes:

vps1 (SPAC767.01c)

Genotypes:

vps1delta

FYPO:0004483 - abnormal vacuole fusion during cellular hypotonic response

References:

Genes:

Genotypes:

FYPO:0006058 - abnormal vacuole fusion during sporulation

References:

PMID:18411246

Genes:

mug27 (SPCC417.06c)

Genotypes:

mug27delta

FYPO:0004482 - abnormal vacuole fusion during vegetative growth

References:

Genes:

Genotypes: