Genopathy
Gene-Disorder Association · Article
Gene
IL10RB
Interleukin 10 Receptor Subunit Beta
Disorder
Inflammatory Bowel Disease 25, Autosomal Recessive
First reported 2018
Supporting publications 8
Key publication · gene–disorder Copy number variations and founder effect underlying complete IL-10Rβ deficiency in Portuguese kindreds.PloS one · 2018
Key publication · disorder Splicing in action: assessing disease causing sequence changes.Journal of medical genetics · 2005
Manually curated
Association Review

In brief

The association between IL10RB (Interleukin 10 Receptor Subunit Beta) and Inflammatory Bowel Disease 25, Autosomal Recessive is well established and manually curated, with its 2 contributing sources — 2 of them expert-curated — recording a known molecular basis and likely-pathogenic variants.

Sources 2
Clinical variants 238
Symptoms 10
Compounds 0
Trials 0
Publications 8
01
At a glance

Association overview

A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.

Request access
02
Provenance

Evidence and sources

2 sources

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

Request access
03
IL10RB

The gene

1 source summary

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

Request access
04
Inflammatory Bowel Disease 25, Autosomal Recessive

The disorder

6 database identifiers

The disorder’s summary, prevalence, aliases and cross-reference identifiers (OMIM, Orphanet, MONDO, ICD-10, MedGen).

Request access
05
Phenotype

Clinical features

7 clinical features

The disorder’s clinical features (HPO) grouped by body system, each with observed frequency and penetrance.

Request access
06
ClinVar and variant evidence

Genetic basis

238 clinical variants

ClinVar variants reported for this pair, with disorder-specific significance, review status, molecular consequence and origin.

Request access
07
Population genetics

GWAS signals

1 GWAS phenotype

Gene-associated GWAS phenotypes matching the disorder, with best SNP, score, risk-allele frequency and effect size.

Request access
08
Mechanism overlap

Shared mechanisms

Biological pathways and phenotype concepts shared by the gene and the disorder, with supporting publications.

Request access
09
Literature

Reading

8 publications

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

Request access
10
Provenance

References & sources

13 references

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

Request access