Genopathy
Gene-Disorder Association · Article
Gene
PAX5
Paired Box 5
Disorder
B-Lymphoblastic Leukemia/Lymphoma With T(7;9)(Q11.2;P13.2)
First reported 2007
Supporting publications 3
Key publication · disorder A novel PAX5-ELN fusion protein identified in B-cell acute lymphoblastic leukemia acts as a dominant negative on wild-type PAX5.Blood · 2007
Manually curated
Association Review

In brief

The association between PAX5 (Paired Box 5) and B-Lymphoblastic Leukemia/Lymphoma With T(7;9)(Q11.2;P13.2) is a manually-curated gene–disease association, supported by a single expert-curated source.

Sources 1
Clinical variants 0
Symptoms 0
Compounds 0
Trials 0
Publications 3
01
At a glance

Association overview

A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.

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02
Provenance

Evidence and sources

1 source

Every contributing database and publication behind this association, with evidence type, strength, accessions and deep links.

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03
PAX5

The gene

1 source summary

A gene summary alongside the source descriptions it was distilled from.

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04
B-Lymphoblastic Leukemia/Lymphoma With T(7;9)(Q11.2;P13.2)

The disorder

4 database identifiers

The disorder’s summary, prevalence, aliases and cross-reference identifiers (OMIM, Orphanet, MONDO, ICD-10, MedGen).

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05
Literature

Reading

3 publications

Publications linking the gene and the disorder, with title, authors, journal, year and citation metrics.

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06
Provenance

References & sources

5 references

Every source and publication cited across this dossier, as one numbered reference list.

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