Phenotype ontology term - FYPO:0003564 - abnormal meiotic DNA double-strand break formation

Term summary

ID: FYPO:0003564
Name: abnormal meiotic DNA double-strand break formation
Ontology or CV name: Phenotype
Definition: A cellular process phenotype in which generation of double-strand breaks at defined hotspots throughout the genome during meiosis I is abnormal.

Parents

is_a abnormal meiotic recombination

Annotation

Multi-locus phenotype

FYPO:0003564 - abnormal meiotic DNA double-strand break formation

References:

PMID:25579976

Genes:

Genotypes:

hhp1+(wild type)[Knockdown] hhp2delta

FYPO:0003181 - abolished meiotic DNA double-strand break formation

References:

PMID:18378696

Genes:

Genotypes:

ctp1delta rec12delta

FYPO:0005137 - delayed onset of meiotic DNA double-strand break formation

References:

PMID:15238514

Genes:

Genotypes:

dmc1delta rad51delta

Single locus phenotype

FYPO:0003564 - abnormal meiotic DNA double-strand break formation

References:

Genes:

Genotypes:

FYPO:0003181 - abolished meiotic DNA double-strand break formation

References:

Genes:

Genotypes:

FYPO:0007237 - increased meiotic DNA double-strand break formation near existing double-strand break

References:

PMID:30217891

Genes:

tel1 (SPCC23B6.03c)

Genotypes:

tel1delta