Human Gene Set: HP_ABNORMAL_T_CELL_APOPTOSIS


Standard name HP_ABNORMAL_T_CELL_APOPTOSIS
Systematic name M48865
Brief description Abnormal T cell apoptosis
Full description or abstract Abnormal apoptosis by peripheral blood T cells in an in vitro culture, compared to a healthy control sample. May be either spontaneous, induced by UV, X-ray, FasL or other agens. Commonly measured by surface expression of phosphatidyl serine labelled by Annexin V, but other methods such as staning of cleaved Caspases may be used by different laboratories. [https://orcid.org/0000-0002-0736-9199, PMID:17562483]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0030886
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0030886
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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
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Version history 2026.1.Hs: Updated to HPO Release 2026-01-08.


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