Genopathy
Gene-Disorder Association · Article
Gene
SLC2A2
Solute Carrier Family 2 Member 2
Disorder
Glycogen Storage Disease
First reported 1999
Supporting publications 3
Key publication · gene–disorder A mutation in GLUT2, not in phosphorylase kinase subunits, in hepato-renal glycogenosis with Fanconi syndrome and low phosphorylase kinase activity.Human genetics · 1999
Key publication · disorder Glycogen storage disease of the heart. II. Critical review of the literature.Pediatrics · 1950
Manually curated
Association Review

In brief

The association between SLC2A2 (Solute Carrier Family 2 Member 2) and Glycogen Storage Disease is reported, with clinical genetic testing available.

Sources 1
Clinical variants 0
Symptoms 0
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

1 source

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

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03
SLC2A2

The gene

1 source summary

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

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04
Glycogen Storage Disease

The disorder

9 database identifiers

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

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05
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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06
Literature

Reading

3 publications

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

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07
Provenance

References & sources

7 references

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

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