Genopathy
Gene-Disorder Association · Article
Gene
PDE6G
Phosphodiesterase 6G
Disorder
Retinitis Pigmentosa 57
First reported 2010
Supporting publications 1
Key publication · gene–disorder Autosomal-recessive early-onset retinitis pigmentosa caused by a mutation in PDE6G, the gene encoding the gamma subunit of rod cGMP phosphodiesterase.American journal of human genetics · 2010
Key publication · disorder The differential diagnosis of visual disorders in patients presenting with marked symptoms but with no observable ocular abnormality.American journal of optometry and physiological optics · 1980
Manually curated
Association Review

In brief

The association between PDE6G (Phosphodiesterase 6G) and Retinitis Pigmentosa 57 is well established and manually curated, with its 3 contributing sources — 2 of them expert-curated — recording a known molecular basis and pathogenic variants.

Sources 3
Clinical variants 3
Symptoms 13
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

3 sources

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

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03
PDE6G

The gene

2 source summaries

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

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04
Retinitis Pigmentosa 57

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

8 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

3 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

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

7 references

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

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