Trait
Decreased memory B cell proportion
A reduction in the normal proportion of memory B cells (CD19+/CD27+) in circulation relative to the total number of B cells. Memory B cells develop from naive B cells. Upon antigen rechallenge, memory B cells rapidly expand and differentiate into plasma cells under the cognate control of memory Th cells (Phase IV).
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- Kabuki SyndromeReads 2 of these genesKDM6AKMT2DAbout this report →
- Hepatic Veno-Occlusive Disease with Immunodeficiency (VODI)Reads 1 of these genesSP110About this report →
- Other Inborn Errors of ImmunityReads 6 of these genesBACH2CTPS1IKBKBIRF4PRKCDSP110About this report →
- Systemic Lupus ErythematosusReads 1 of these genesPRKCDAbout this report →
Show 6 more reports
- Autoimmune Lymphoproliferative Syndrome (ALPS)Reads 1 of these genesPRKCDAbout this report →
- IPEX Syndrome and Other TregopathiesReads 1 of these genesBACH2About this report →
- Severe Combined ImmunodeficiencyReads 2 of these genesCTPS1IKBKBAbout this report →
- Rare Monogenic Autoinflammatory DiseasesReads 2 of these genesELF4POMPAbout this report →
- Type I InterferonopathiesReads 1 of these genesPOMPAbout this report →
- Autoimmune DiseaseReads 1 of these genesPRKCDAbout this report →
Read the genes linked to Decreased memory B cell proportion, and the rest of your genome, with one test.
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Get my Genome Test13 genes linked to Decreased memory B cell proportion
Changes in these genes cause rare conditions in which Decreased memory B cell proportion 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 |
|---|---|---|
| ARHGEF1Rho guanine nucleotide exchange factor 1 | Always | In 1 condition |
| BACH2BACH transcriptional regulator 2 | Always | In 1 condition |
| CTPS1CTP synthase 1 | Always | In 1 condition |
| ELF4E74 like ETS transcription factor 4 | Always | In 1 condition |
| IKBKBinhibitor of nuclear factor kappa B kinase subunit beta | Always | In 1 condition |
| IRF4interferon regulatory factor 4 | Always | In 1 condition |
| POMPproteasome maturation protein | Always | In 1 condition |
| PRKCDprotein kinase C delta | Always | In 1 condition |
| KDM6Alysine demethylase 6A | Very often (80–99%) | In 1 condition |
| KMT2Dlysine methyltransferase 2D | Very often (80–99%) | In 1 condition |
| IL27RAinterleukin 27 receptor subunit alpha | Often (30–79%) | In 1 condition |
| SP110SP110 nuclear body protein | Often (30–79%) | In 1 condition |
| TOM1target of myb1 membrane trafficking protein | 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 2026.10.19-9814e911.
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