Genopathy
Gene-Disorder Association · Article
Gene
MNX1-AS2
MNX1 Antisense RNA 2
Disorder
Currarino Syndrome
First reported 1974
Supporting publications 4
Key publication · disorder Hereditary presacral teratoma.Journal of pediatric surgery · 1974
Association Review

In brief

The association between MNX1-AS2 (MNX1 Antisense RNA 2) and Currarino Syndrome is supported by expert-curated evidence, drawing on a single expert-curated source, which records pathogenic variants.

Sources 1
Clinical variants 10
Symptoms 65
Compounds 0
Trials 0
Publications 4
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
MNX1-AS2

The gene

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

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04
Currarino Syndrome

The disorder

16 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

53 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

10 clinical variants

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

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07
Literature

Reading

4 publications

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

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08
Provenance

References & sources

9 references

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

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