Genopathy
Gene-Disorder Association · Article
Gene
LFNG
LFNG O-Fucosylpeptide 3-Beta-N-Acetylglucosaminyltransferase
Disorder
Spondylocostal Dysostosis 3, Autosomal Recessive
First reported 2019
Supporting publications 4
Key publication · gene–disorder Identification of novel LFNG mutations in spondylocostal dysostosis.Journal of human genetics · 2019
Key publication · disorder Mutated MESP2 causes spondylocostal dysostosis in humans.American journal of human genetics · 2004
Manually curated
Association Review

In brief

The association between LFNG (LFNG O-Fucosylpeptide 3-Beta-N-Acetylglucosaminyltransferase) and Spondylocostal Dysostosis 3, Autosomal Recessive is well established and manually curated, with its 4 contributing sources — 3 of them expert-curated — recording a known molecular basis, likely-pathogenic variants, and causative variation.

Sources 4
Clinical variants 220
Symptoms 17
Compounds 0
Trials 0
Publications 4
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

4 sources

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

Request access
03
LFNG

The gene

1 source summary

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

Request access
04
Spondylocostal Dysostosis 3, Autosomal Recessive

The disorder

8 database identifiers

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

Request access
05
Phenotype

Clinical features

9 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

220 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

4 publications

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

Request access
09
Provenance

References & sources

14 references

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

Request access