Genopathy
Gene-Disorder Association · Article
Gene
NUS1
NUS1 Dehydrodolichyl Diphosphate Synthase Subunit
Disorder
Intellectual Developmental Disorder, Autosomal Dominant 55, With Seizures
First reported 1984
Supporting publications 4
Key publication · disorder Macrocephaly with hamartomas: Bannayan-Zonana syndrome.American journal of medical genetics · 1984
Manually curated
Association Review

In brief

The association between NUS1 (NUS1 Dehydrodolichyl Diphosphate Synthase Subunit) and Intellectual Developmental Disorder, Autosomal Dominant 55, With Seizures is well established and manually curated, with its 3 contributing sources — 2 of them expert-curated — recording a known molecular basis and pathogenic variants.

Sources 3
Clinical variants 38
Symptoms 28
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

3 sources

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

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03
NUS1

The gene

1 source summary

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

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04
Intellectual Developmental Disorder, Autosomal Dominant 55, With Seizures

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

17 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

38 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

4 publications

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

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09
Provenance

References & sources

9 references

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

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