Genopathy
Gene-Disorder Association · Article
Gene
PAPSS2
3'-Phosphoadenosine 5'-Phosphosulfate Synthase 2
Disorder
Autosomal Recessive Brachyolmia
First reported 2009
Supporting publications 2
Key publication · disorder Inactivating PAPSS2 mutations in a patient with premature pubarche.The New England journal of medicine · 2009
Manually curated
Association Review

In brief

The association between PAPSS2 (3'-Phosphoadenosine 5'-Phosphosulfate Synthase 2) and Autosomal Recessive Brachyolmia is well established and manually curated, with its 2 contributing sources — 2 of them expert-curated — recording pathogenic variants and a causative germline mutation.

Sources 2
Clinical variants 1
Symptoms 0
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.

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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
PAPSS2

The gene

1 source summary

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

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04
Autosomal Recessive Brachyolmia

The disorder

5 database identifiers

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

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05
ClinVar and variant evidence

Genetic basis

1 clinical variant

ClinVar variants reported for this pair, with disorder-specific significance, review status, molecular consequence and origin.

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06
Literature

Reading

2 publications

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

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07
Provenance

References & sources

6 references

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

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