Genopathy
Gene-Disorder Association · Article
Gene
SDCCAG8
SHH Signaling And Ciliogenesis Regulator SDCCAG8
Disorder
Bardet-Biedl Syndrome 16
First reported 2011
Supporting publications 12
Key publication · gene–disorder Mutations in SDCCAG8/NPHP10 Cause Bardet-Biedl Syndrome and Are Associated with Penetrant Renal Disease and Absent Polydactyly.Molecular syndromology · 2011
Key publication · disorder The Laurence-Moon-Bardet-Biedl syndrome: unresponsiveness to the action of testosterone, a possible mechanism.Fertility and sterility · 1979
Manually curated
Association Review

In brief

The association between SDCCAG8 (SHH Signaling And Ciliogenesis Regulator SDCCAG8) and Bardet-Biedl Syndrome 16 is well established and manually curated, with its 3 contributing sources — 2 of them expert-curated — recording a known molecular basis and likely-pathogenic variants.

Sources 3
Clinical variants 595
Symptoms 35
Compounds 0
Trials 0
Publications 12
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
SDCCAG8

The gene

1 source summary

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

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04
Bardet-Biedl Syndrome 16

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

21 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

595 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

12 publications

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

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09
Provenance

References & sources

14 references

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

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