Genopathy
Gene-Disorder Association · Article
Gene
RNU6-8
RNA, U6 Small Nuclear 8
Disorder
Retinitis Pigmentosa 105
First reported 1995
Key publication · disorder RP105, a novel B cell surface molecule implicated in B cell activation, is a member of the leucine-rich repeat protein family.Journal of immunology (Baltimore, Md. : 1950) · 1995
Manually curated
Association Review

In brief

The association between RNU6-8 (RNA, U6 Small Nuclear 8) and Retinitis Pigmentosa 105 is a manually-curated gene–disease association, drawing on a single expert-curated source, which records a known molecular basis.

Sources 1
Clinical variants 0
Symptoms 0
Compounds 0
Trials 0
Publications 0
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
RNU6-8

The gene

1 source summary

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

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04
Retinitis Pigmentosa 105

The disorder

2 database identifiers

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

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05
Provenance

References & sources

2 references

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

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