Genopathy
Gene-Disorder Association · Article
Gene
RAP1B
RAP1B, Member Of RAS Oncogene Family
Disorder
Thrombocytopenia 11 With Multiple Congenital Anomalies And Dysmorphic Facies
First reported 1996
Supporting publications 3
Key publication · disorder The v-erbB oncogene confers enhanced cellular susceptibility to reovirus infection.Journal of virology · 1996
Manually curated
Association Review

In brief

The association between RAP1B (RAP1B, Member Of RAS Oncogene Family) and Thrombocytopenia 11 With Multiple Congenital Anomalies And Dysmorphic Facies is well established and manually curated, with its 3 contributing sources — 3 of them expert-curated — recording a known molecular basis, likely-pathogenic variants, and causative variation.

Sources 3
Clinical variants 7
Symptoms 123
Compounds 0
Trials 0
Publications 3
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
RAP1B

The gene

1 source summary

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

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04
Thrombocytopenia 11 With Multiple Congenital Anomalies And Dysmorphic Facies

The disorder

7 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

72 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

7 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

3 publications

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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