Genopathy
Gene-Disorder Association · Article
Gene
CEP19
Centrosomal Protein 19
Disorder
Bardet-Biedl Syndrome
First reported 2018
Supporting publications 1
Key publication · gene–disorder Homozygous mutation in CEP19, a gene mutated in morbid obesity, in Bardet-Biedl syndrome with predominant postaxial polydactyly.Journal of medical genetics · 2018
Key publication · disorder [Laurence-Moon-Bardet-Biedl syndrome].Revue d'oto-neuro-ophtalmologie · 1950
Manually curated
Association Review

In brief

The association between CEP19 (Centrosomal Protein 19) and Bardet-Biedl Syndrome is well established and manually curated, with its 3 contributing sources — 2 of them expert-curated — recording pathogenic variants and a causative germline mutation.

Sources 3
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

3 sources

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

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03
CEP19

The gene

1 source summary

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

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04
Bardet-Biedl Syndrome

The disorder

9 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

95 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

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

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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