The NCF2 gene homepage

General information
Gene symbol NCF2
Gene name neutrophil cytosolic factor 2
Chromosome 1
Chromosomal band q25
Imprinted Unknown
Genomic reference LRG_88
Transcript reference NM_000433.3
Exon/intron information NM_000433.3 exon/intron table
Associated with diseases CGD, CGD2
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 184
Unique public DNA variants reported 92
Individuals with public variants 244
Hidden variants -
Download all this gene's data Download all data
Notes Establishment of this gene variant database (LSDB) was performed by Johan den Dunnen, supported by Global Variome.
Date created May 03, 2013
Date last updated November 27, 2023
Version NCF2:231127

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
Reading frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes. Active for: NM_000433.3.
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
Homepage URL https://www.LOVD.nl/NCF2
HGNC 7661
Entrez Gene 4688
PubMed articles NCF2
OMIM - Gene 608515
OMIM - Diseases CGD2 (granulomatous disease, chronic, due to deficiency of NCF-2, type 2)
HGMD NCF2
GeneCards NCF2
GeneTests NCF2
Orphanet NCF2


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00014349 1 transcript variant 1 NM_000433.3 NP_000424.2 184


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