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NCF1

neutrophil cytosolic factor 1
2 disorders 1 causative 1 susceptibility 7q11.23 gene with protein product
HGNC:7660MonarchNCBI Gene 653361ENSG00000158517UniProt P14598OMIM 608512

Aliases: p47phox, NOXO2, NCF1A, SH3PXD1A.

In the knowledge base · computed from kb/ at build time

Disorders

Relationship is the entry's genetic[].relationship_type. untyped means the entry has a genetic record for the gene but does not type it; its free-text association is shown instead.

DisorderRelationshipWhere the gene appears
Chronic Granulomatous Disease causative
mechanism: NADPH oxidase (NOX2) complex assembly failure
subtype: AR p47phox NCF1
scoped to subtype: AR p47phox NCF1
Invasive Non-Typhoidal Salmonellosis susceptibility
Mechanism modules · computed from kb/

Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.