Trait
Abnormal T cell proliferation
Any abnormality in the multiplication or reproduction of T cells, which results in the expansion of a cell population.
Summary
- Also called
- Defective T cell proliferation
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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Get my Genome Test8 genes linked to Abnormal T cell proliferation
Changes in these genes cause rare conditions in which Abnormal T cell proliferation is seen. Most people with this trait have none of those conditions, and a gene on this list says nothing about anyone's own genome.
| Gene | How often it is seen | Conditions |
|---|---|---|
| CD3ECD3 epsilon subunit of T-cell receptor complex | Always | In 1 condition |
| LATlinker for activation of T cells | Always | In 1 condition |
| LIG1DNA ligase 1 | Always | In 1 condition |
| MRTFAmyocardin related transcription factor A | Always | In 1 condition |
| RASGRP1RAS guanyl releasing protein 1 | Always | In 1 condition |
| WIPF1WAS/WASL interacting protein family member 1 | Always | In 1 condition |
| CTPS1CTP synthase 1 | Sometimes (5–29%) | In 1 condition |
| TGFB1transforming growth factor beta 1 | Not recorded | In 1 condition |
How often is among people with one of the gene's conditions, the most often across them, as the Human Phenotype Ontology records it. These pages describe traits and the research behind them; they are not a diagnosis, and a doctor or genetic counsellor is the person to ask about symptoms.
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Where this comes from
- The Human Phenotype Ontology, release 2026-09-01: the trait, its names, its definition and the genes linked to it. Find out more at hpo.jax.org.
- Data release 2026.10.16-c6eea6bf.
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