Genopathy
Gene-Disorder Association · Article
Gene
SLC6A3
Solute Carrier Family 6 Member 3
Disorder
Parkinsonism-Dystonia 1, Infantile-Onset
First reported 2009
Supporting publications 3
Key publication · gene–disorder Homozygous loss-of-function mutations in the gene encoding the dopamine transporter are associated with infantile parkinsonism-dystonia.The Journal of clinical investigation · 2009
Key publication · disorder Occupational allergic contact dermatitis to isophorone diamine (IPD) used as an epoxy resin hardener.Contact dermatitis · 1978
Manually curated
Association Review

In brief

The association between SLC6A3 (Solute Carrier Family 6 Member 3) and Parkinsonism-Dystonia 1, Infantile-Onset is well established and manually curated, with its 3 contributing sources — 3 of them expert-curated — recording a known molecular basis, likely-pathogenic variants, and causative variation.

Sources 3
Clinical variants 41
Symptoms 37
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

3 sources

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

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03
SLC6A3

The gene

2 source summaries

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

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04
Parkinsonism-Dystonia 1, Infantile-Onset

The disorder

8 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

24 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

41 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

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

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08
Literature

Reading

3 publications

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

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09
Provenance

References & sources

9 references

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

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