Phenotype ontology term - FYPO:0005652 - abnormal spindle morphology during meiosis I

Term summary

ID: FYPO:0005652
Name: abnormal spindle morphology during meiosis I
Ontology or CV name: Phenotype
Definition: A physical cellular phenotype in which the size, shape, or structure of the spindle is abnormal during the first meiotic nuclear division.

Parents

is_a abnormal spindle morphology

Annotation

Multi-locus phenotype

FYPO:0005652 - abnormal spindle morphology during meiosis I

References:

Genes:

Genotypes:

FYPO:0006363 - monopolar spindle during meiosis I

References:

Genes:

Genotypes:

FYPO:0006364 - spindle microtubules detached from spindle pole body during meiosis I

References:

PMID:17632059

Genes:

Genotypes:

lig4delta taz1delta

Single locus phenotype

FYPO:0005652 - abnormal spindle morphology during meiosis I

References:

PMID:21084840

Genes:

rdh54 (SPAC22F3.03c)

Genotypes:

rdh54-70%-deleted

FYPO:0006363 - monopolar spindle during meiosis I

References:

Genes:

Genotypes:

FYPO:0006364 - spindle microtubules detached from spindle pole body during meiosis I

References:

PMID:24954111

Genes:

bqt2 (SPAC1002.06c)

Genotypes:

bqt2delta