Genopathy
Gene-Disorder Association · Article
Gene
NCF2
Neutrophil Cytosolic Factor 2
Disorder
Chronic Granulomatous Disease
First reported 1990
Supporting publications 32
Key publication · gene–disorder Genes for two autosomal recessive forms of chronic granulomatous disease assigned to 1q25 (NCF2) and 7q11.23 (NCF1).American journal of human genetics · 1990
Key publication · disorder A fatal granulomatous disease of childhood; the clinical, pathological, and laboratory features of a new syndrome.A.M.A. journal of diseases of children · 1959
Manually curated
Association Review

In brief

The association between NCF2 (Neutrophil Cytosolic Factor 2) and Chronic Granulomatous Disease is well established and manually curated, with its 3 contributing sources — 2 of them expert-curated — recording pathogenic variants and a causative germline mutation.

Sources 3
Clinical variants 19
Symptoms 22
Compounds 0
Trials 0
Publications 32
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
NCF2

The gene

1 source summary

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

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04
Chronic Granulomatous Disease

The disorder

12 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

22 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

19 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

1 shared pathway

Biological pathways and phenotype concepts shared by the gene and the disorder, with supporting publications.

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08
Literature

Reading

32 publications

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

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09
Provenance

References & sources

18 references

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

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