Genopathy
Gene-Disorder Association · Article
Gene
RAB9B
RAB9B, Member RAS Oncogene Family
First reported 1960
Supporting publications 81
Manually curated
Association Review

In brief

The association between RAB9B (RAB9B, Member RAS Oncogene Family) and Pelizeaus-Merzbacher Spectrum Disorder is well established and manually curated, drawing on a single expert-curated source, which records likely-pathogenic variants.

Sources 1
Clinical variants 157
Symptoms 0
Compounds 0
Trials 0
Publications 81
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

1 source

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

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03
RAB9B

The gene

1 source summary

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

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04
Pelizeaus-Merzbacher Spectrum Disorder

The disorder

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

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05
ClinVar and variant evidence

Genetic basis

157 clinical variants

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

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06
Literature

Reading

81 publications

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

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07
Provenance

References & sources

10 references

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

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