Genopathy
Gene-Disorder Association · Article
Gene
SLX4
SLX4 Structure-Specific Endonuclease Subunit
Disorder
Fanconi Anemia, Complementation Group A
First reported 2011
Supporting publications 19
Key publication · gene–disorder Mutations of the SLX4 gene in Fanconi anemia.Nature genetics · 2011
Key publication · disorder A case of Fanconi's anaemia.Archives of disease in childhood · 1951
Manually curated
Association Review

In brief

The association between SLX4 (SLX4 Structure-Specific Endonuclease Subunit) and Fanconi Anemia, Complementation Group A is well established and manually curated, with its 3 contributing sources — 2 of them expert-curated — recording pathogenic and likely-pathogenic variants and a causative germline mutation.

Sources 3
Clinical variants 2,033
Symptoms 159
Compounds 0
Trials 0
Publications 19
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

3 sources

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

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03
SLX4

The gene

1 source summary

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

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04
Fanconi Anemia, Complementation Group A

The disorder

17 database identifiers

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

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05
Phenotype

Clinical features

129 clinical features

The disorder’s clinical features (HPO) grouped by body system, each with observed frequency and penetrance.

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06
ClinVar and variant evidence

Genetic basis

2,033 clinical variants

ClinVar variants reported for this pair, with disorder-specific significance, review status, molecular consequence and origin.

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07
Mechanism overlap

Shared mechanisms

1 shared pathway

Biological pathways and phenotype concepts shared by the gene and the disorder, with supporting publications.

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08
Literature

Reading

19 publications

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

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09
Provenance

References & sources

19 references

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

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