Genopathy
Gene-Disorder Association · Article
Gene
AGPAT2
1-Acylglycerol-3-Phosphate O-Acyltransferase 2
Disorder
Congenital Generalized Lipodystrophy
First reported 2002
Supporting publications 13
Key publication · gene–disorder AGPAT2 is mutated in congenital generalized lipodystrophy linked to chromosome 9q34.Nature genetics · 2002
Key publication · disorder Generalized lipodystrophy, infectious mononucleosis, mild infantile hemiplegia.Proceedings of the Royal Society of Medicine · 1954
Manually curated
Association Review

In brief

The association between AGPAT2 (1-Acylglycerol-3-Phosphate O-Acyltransferase 2) and Congenital Generalized Lipodystrophy is well established and manually curated, with its 2 contributing sources — 1 of them expert-curated — recording pathogenic variants.

Sources 2
Clinical variants 7
Symptoms 38
Compounds 0
Trials 0
Publications 13
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

2 sources

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

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03
AGPAT2

The gene

1 source summary

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

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04
Congenital Generalized Lipodystrophy

The disorder

10 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

37 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

7 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

13 publications

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

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09
Provenance

References & sources

19 references

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

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