| GENE NAME | NCF2 |
| CHROMOSOME | 1 |
| ENSEMBL ID | None |
| ENTREZ ID | ENSG00000116701 |
| UNIPROT ACCESSION NUMBER | P19878 |
| GO MOLECULAR FUNCTION | ['small GTPase binding', 'electron transfer activity', 'protein C-terminus binding', 'protein binding', 'superoxide-generating NADPH oxidase activator activity', 'superoxide-generating NAD(P)H oxidase activity'] |
| ESSENTIAL IN MOUSE | None |
| PATHWAYS | hsa04145; hsa04380; hsa04613; hsa04670; hsa05020; hsa05140; hsa05418; hsa04145; hsa04380; hsa04613; hsa04670; hsa05020; hsa05140; hsa05418; R-HSA-1222556; R-HSA-1236973; R-HSA-1236975; R-HSA-1280218; R-HSA-162582; R-HSA-168249; R-HSA-168256; R-HSA-194138; R-HSA-194315; R-HSA-195258; R-HSA-2262752; R-HSA-3299685; R-HSA-4420097; R-HSA-5668599; R-HSA-8953897; R-HSA-9006934; R-HSA-983169 |
| 1 combination linked to NCF2 | OLI1716 |
| 1 variant linked to NCF2 | NCF2:p.Phe116Ser |
| 1 disease linked to NCF2 | Common variable immunodeficiency |