Human Gene Set: HP_ABNORMAL_T_CELL_ACTIVATION


Standard name HP_ABNORMAL_T_CELL_ACTIVATION
Systematic name M48931
Brief description Abnormal T cell activation
Full description or abstract Any abnormality in the activation of T cells, i.e. the change in morphology and behavior of a mature or immature T cell resulting from exposure to a mitogen, cytokine, chemokine, cellular ligand, or an antigen for which it is specific. []
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0410035
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0410035
Filtered by similarity ? (show 1 similar ontology term(s) from the external resource)
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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GTEx compendium
Human tissue compendium (Novartis)
Global Cancer Map (Broad Institute)
NCI-60 cell lines (National Cancer Institute)
Advanced query Further investigate these 9 genes
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Version history 2024.1.Hs: Updated to HPO Release 2024-04-26.

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