Trait
High blood monocyte number
Clinical name: Increased total monocyte count
Abnormal increase of absolute number of monocytes in the blood, per microlitre, compared to a reference range for a given sex and age-group.
Summary
- Also called
- Monocytosis
Read the genes linked to High blood monocyte number, and the rest of your genome, with one test.
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Get my Genome Test18 genes linked to High blood monocyte number
Changes in these genes cause rare conditions in which High blood monocyte number 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 |
|---|---|---|
| ARPC5actin related protein 2/3 complex subunit 5 | Always | In 1 condition |
| COPZ1coat protein complex I subunit zeta 1 | Always | In 1 condition |
| OTULINOTU deubiquitinase with linear linkage specificity | Always | In 1 condition |
| PIK3CDphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta | Always | In 1 condition |
| SEC61A1SEC61 translocon subunit alpha 1 | Always | In 1 condition |
| SRP68signal recognition particle 68 | Always | In 1 condition |
| TMEM63Btransmembrane protein 63B | Always | In 1 condition |
| CLPBClpB family mitochondrial disaggregase | Often (30–79%) | In 1 condition |
| ELANEelastase, neutrophil expressed | Often (30–79%) | In 2 conditions |
| GFI1growth factor independent 1 transcriptional repressor | Often (30–79%) | In 2 conditions |
| IKBKBinhibitor of nuclear factor kappa B kinase subunit beta | Often (30–79%) | In 1 condition |
| SRP19signal recognition particle 19 | Often (30–79%) | In 1 condition |
| TAFAZZINtafazzin, phospholipid-lysophospholipid transacylase | Often (30–79%) | In 1 condition |
| TCIRG1T cell immune regulator 1, ATPase H+ transporting V0 subunit a3 | Often (30–79%) | In 1 condition |
| ZNFX1zinc finger NFX1-type containing 1 | Often (30–79%) | In 1 condition |
| DDX41DEAD-box helicase 41 | Not recorded | In 1 condition |
| G6PC3glucose-6-phosphatase catalytic subunit 3 | Not recorded | In 1 condition |
| NRASNRAS proto-oncogene, GTPase | 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.
Broader traits
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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