Human Gene Set: HP_CHROMOSOME_BREAKAGE


Standard name HP_CHROMOSOME_BREAKAGE
Systematic name M38563
Brief description Chromosome breakage
Full description or abstract Elevated rate of chromosomal breakage or interchanges occurring either spontaneously or following exposure to various DNA-damaging agents. This feature may be assayed by treatment of cultured lymphocytes with agents such as chemical mutagens, irradiation, and alkylating agents. [https://orcid.org/0000-0002-0736-9199, PMID:12407692]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0040012
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0040012
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Source species Homo sapiens
Contributed by Human Phenotype Ontology Group (The Jackson Laboratory (JAX))
Source platform or
identifier namespace		 Human_NCBI_Gene_ID
Dataset references  
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GTEx compendium
Human tissue compendium (Novartis)
Global Cancer Map (Broad Institute)
NCI-60 cell lines (National Cancer Institute)
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Version history 2023.1.Hs: Updated to HPO Release 2023-01-27.

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