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Symbol report for NCF2

HGNC data for NCF2

Approved symbol
NCF2
Approved name

neutrophil cytosolic factor 2

Locus type
gene with protein product
HGNC ID
HGNC:7661
Symbol status
Approved
Previous names
neutrophil cytosolic factor 2 (65kD, chronic granulomatous disease, autosomal 2)
Alias symbols
p67phox
NOXA2
Alias names
NADPH oxidase activator 2
chronic granulomatous disease, autosomal 2
Chromosomal location
1q25.3
Gene groups
Gene resources for NCF2
Ensembl
ENSG00000116701 Curated
Ensembl region in detailEnsembl gene sequence
NCBI Gene
4688 Curated
UCSC
uc001gqk.5
Alliance of Genome Resources
HGNC:7661
Nucleotide resources for NCF2
MANE Select
NM_000433.4
ENST00000367535.8
INSDC
BC001606 Curated
ENAGenBankDDBJ
RefSeq
NM_000433 Curated
NCBI sequence viewer
Protein resources for NCF2
UniProt/Swiss-Prot
P19878
InterProPDBeReactome
AlphaFold
AF-P19878-F1
Orthologs from selected species for NCF2
Bos taurus
NCF2 VGNC:31912 VGNC
Canis familiaris
NCF2 VGNC:43650 VGNC
Equus caballus
NCF2 VGNC:20586 VGNC
Felis catus
NCF2 VGNC:68425 VGNC
Macaca mulatta
NCF2 VGNC:75140 VGNC
Mus musculus
Ncf2 MGI:97284 Curated
Pan troglodytes
NCF2 VGNC:1343 VGNC
Rattus norvegicus
Ncf2 RGD:1309424
Sus scrofa
NCF2 VGNC:90607 VGNC
Clinical resources for NCF2
OMIM
608515
LRG
LRG_88 Curated
LSDB
NCF2base: Mutation registry for autosomal recessive chronic granulomatous disease (CGD), deficiency of p67phox Curated
GenCC
HGNC:7661
MedlinePlus
Search via NCF2
DECIPHER
Search via NCF2
ClinGen
Search via HGNC:7661
Genetic Testing Registry
Search via NCBI Gene ID 4688
ClinVar
Search via NCBI Gene ID 4688
dbVar
Search via NCBI Gene ID 4688
Orphanet
123701
Other resources for NCF2
AmiGO
Search via P19878
QuickGO
Search via P19878
BioGPS
Search via NCBI Gene ID 4688
GeneCards
Search via HGNC:7661
Monarch
Search via HGNC:7661
WikiGenes
Search via NCBI Gene ID 4688