Genopathy
Gene-Disorder Association · Article
Gene
UGT1A1
UDP Glucuronosyltransferase Family 1 Member A1
Disorder
Gilbert Syndrome
First reported 1995
Supporting publications 66
Key publication · gene–disorder The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert's syndrome.The New England journal of medicine · 1995
Key publication · disorder Hyperbilirubinemia. I. A rapid screening test for its detection.The Journal of laboratory and clinical medicine · 1951
Manually curated
Association Review

In brief

The association between UGT1A1 (UDP Glucuronosyltransferase Family 1 Member A1) and Gilbert Syndrome is well established and manually curated, with its 4 contributing sources — 3 of them expert-curated — recording a known molecular basis, pathogenic and likely-pathogenic variants, and causative variation.

Sources 4
Clinical variants 108
Symptoms 7
Compounds 0
Trials 0
Publications 66
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

4 sources

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

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03
UGT1A1

The gene

1 source summary

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

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04
Gilbert Syndrome

The disorder

10 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

4 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

108 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

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

66 publications

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

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09
Provenance

References & sources

18 references

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

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