Genopathy
Gene-Disorder Association · Article
Gene
SLC29A3
Solute Carrier Family 29 Member 3
Disorder
Dysosteosclerosis
First reported 2021
Supporting publications 1
Key publication · gene–disorder Resolution of sclerotic lesions of dysosteosclerosis due to biallelic SLC29A3 variant in a Turkish girl.American journal of medical genetics. Part A · 2021
Key publication · disorder [Dysosteosclerosis--a special form of generalized osteosclerosis].Fortschritte auf dem Gebiete der Rontgenstrahlen und der Nuklearmedizin · 1968
Manually curated
Association Review

In brief

The association between SLC29A3 (Solute Carrier Family 29 Member 3) and Dysosteosclerosis 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 97
Compounds 0
Trials 0
Publications 1
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
SLC29A3

The gene

2 source summaries

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

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04
Dysosteosclerosis

The disorder

8 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

59 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

1 clinical variant

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

1 publication

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

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09
Provenance

References & sources

8 references

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

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