Genopathy
Gene-Disorder Association · Article
Gene
SLC52A2
Solute Carrier Family 52 Member 2
Disorder
Brown-Vialetto-Van Laere Syndrome 2
First reported 2012
Supporting publications 25
Key publication · gene–disorder Exome sequencing reveals riboflavin transporter mutations as a cause of motor neuron disease.Brain : a journal of neurology · 2012
Key publication · disorder Neonatal adrenoleukodystrophy: new cases, biochemical studies, and differentiation from Zellweger and related peroxisomal polydystrophy syndromes.American journal of medical genetics · 1986
Manually curated
Association Review

In brief

The association between SLC52A2 (Solute Carrier Family 52 Member 2) and Brown-Vialetto-Van Laere Syndrome 2 is well established and manually curated, with its 5 contributing sources — 4 of them expert-curated — recording a known molecular basis, pathogenic and likely-pathogenic variants, and a causative germline mutation.

Sources 5
Clinical variants 445
Symptoms 67
Compounds 0
Trials 0
Publications 25
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

5 sources

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

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03
SLC52A2

The gene

1 source summary

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

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04
Brown-Vialetto-Van Laere Syndrome 2

The disorder

18 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

41 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

445 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

25 publications

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

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09
Provenance

References & sources

21 references

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

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