Genopathy
Gene-Disorder Association · Article
Gene
FANCL
FA Complementation Group L
Disorder
Fanconi Anemia, Complementation Group A
First reported 2003
Supporting publications 31
Key publication · gene–disorder A novel ubiquitin ligase is deficient in Fanconi anemia.Nature genetics · 2003
Key publication · disorder A case of Fanconi's anaemia.Archives of disease in childhood · 1951
Manually curated
Association Review

In brief

The association between FANCL (FA Complementation Group L) 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 630
Symptoms 159
Compounds 0
Trials 0
Publications 31
01
At a glance

Association overview

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

Request access
02
Provenance

Evidence and sources

3 sources

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

Request access
03
FANCL

The gene

1 source summary

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

Request access
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).

Request access
05
Phenotype

Clinical features

129 clinical features

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

Request access
06
ClinVar and variant evidence

Genetic basis

630 clinical variants

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

Request access
07
Mechanism overlap

Shared mechanisms

1 shared pathway

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

Request access
08
Literature

Reading

31 publications

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

Request access
09
Provenance

References & sources

19 references

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

Request access