Genopathy
Gene-Disorder Association · Article
Gene
SLC2A1
Solute Carrier Family 2 Member 1
Disorder
Movement Disease
First reported 2004
Supporting publications 2
Key publication · gene–disorder [Type 1 glucose transporter (Glut1) deficiency: manifestations of a hereditary neurological syndrome].Revista de neurologia · 2004
Key publication · disorder [The late result of surgery of extrapyramidal movement disorders and paraplegias].Deutsche Zeitschrift fur Nervenheilkunde · 1952
Manually curated
Association Review

In brief

The association between SLC2A1 (Solute Carrier Family 2 Member 1) and Movement Disease is reported, with clinical genetic testing available.

Sources 1
Clinical variants 0
Symptoms 28
Compounds 0
Trials 0
Publications 2
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

1 source

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

Request access
03
SLC2A1

The gene

2 source summaries

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

Request access
04
Movement Disease

The disorder

6 database identifiers

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

Request access
05
Literature

Reading

2 publications

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

Request access
06
Provenance

References & sources

6 references

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

Request access