Phenotype ontology term - FYPO:0000197 - abnormal horsetail movement

Term summary

ID: FYPO:0000197
Name: abnormal horsetail movement
Ontology or CV name: Phenotype
Definition: A cellular process phenotype in which horsetail movement is abnormal. Horsetail movement is the oscillatory movement of the nucleus that takes place during meiotic prophase I.

Parents

is_a abnormal transport
is_a abnormal meiotic cell cycle process

Annotation

Multi-locus phenotype

FYPO:0000927 - abolished horsetail movement

References:

PMID:17632059

Genes:

Genotypes:

lig4delta rap1delta

FYPO:0004605 - decreased distance travelled by the spindle pole body during horsetail movement

References:

PMID:24954111

Genes:

Genotypes:

FYPO:0004998 - decreased duration of horsetail movement

References:

PMID:25492408

Genes:

Genotypes:

csn1delta mei4+(wild type)[Overexpression]

Single locus phenotype

FYPO:0000197 - abnormal horsetail movement

References:

Genes:

Genotypes:

FYPO:0000927 - abolished horsetail movement

References:

Genes:

Genotypes:

FYPO:0004605 - decreased distance travelled by the spindle pole body during horsetail movement

References:

Genes:

Genotypes:

FYPO:0004998 - decreased duration of horsetail movement

References:

PMID:25492408

Genes:

mei4 (SPBC32H8.11)

Genotypes:

mei4+(wild type)[Overexpression]

FYPO:0004966 - increased duration of horsetail movement

References:

Genes:

Genotypes: