Genopathy
Gene-Disorder Association · Article
Gene
SLC1A3
Solute Carrier Family 1 Member 3
Disorder
Episodic Ataxia, Type 6
First reported 2009
Supporting publications 4
Key publication · gene–disorder Episodic ataxia associated with EAAT1 mutation C186S affecting glutamate reuptake.Archives of neurology · 2009
Key publication · disorder Augmentation of antitumor activity by combined cryo-destruction of sarcoma 180 and protein-bound polysaccharide, EA6, isolated from Flammulina velutipes (Curt. ex Fr.) Sing. in ICR mice.Journal of pharmacobio-dynamics · 1982
Manually curated
Association Review

In brief

The association between SLC1A3 (Solute Carrier Family 1 Member 3) and Episodic Ataxia, Type 6 is well established and manually curated, with its 5 contributing sources — 4 of them expert-curated — recording a known molecular basis, pathogenic variants, and a causative germline mutation.

Sources 5
Clinical variants 102
Symptoms 38
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.

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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
SLC1A3

The gene

2 source summaries

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

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04
Episodic Ataxia, Type 6

The disorder

11 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

25 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

102 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

4 publications

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

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09
Provenance

References & sources

13 references

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

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