common fragile site

A chromosomal fragile site is a specific heritable point on a chromosome that tends to form a gap or constriction and may tend to break when the cell is exposed to partial replication stress.Based on their frequency, fragile sites are classified as common or rare.To date, more than 120 fragile sites have been identified in the human genome.

Identifier
CONSO00158
Type
cellular component
Author
Lingling Xu
ORCID iD iconhttps://orcid.org/0000-0002-0303-8616

References

Cross-references

None available.

Synonyms

None available.

Incoming Relations

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Outgoing Relations

None available.