Genomic Map
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Target Gene Details
Entrez Gene ID: | 4688 |
Gene Name: | neutrophil cytosolic factor 2 |
Gene Aliases: |
NCF-2, NOXA2, P67-PHOX, P67PHOX |
Location: |
Chr.1:183555562-183590921 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 11 - Intron 12 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| NCF2 | NM_000433.3 | NP_000424.2 | ||
| NM_001127651.2 | NP_001121123.1 | |||
| NM_001190789.1 | NP_001177718.1 | |||
| NM_001190794.1 | NP_001177723.1 | |||
| XM_005245207.1 | XP_005245264.1 | |||
| XM_011509580.1 | XP_011507882.1 | |||
| XM_011509581.1 | XP_011507883.1 | |||
| AB209647.1 | BAD92884.1 | |||
| AF527950.1 | AAM89263.1 | |||
| AK296672.1 | ||||
| AK298713.1 | ||||
| AK312666.1 | ||||
| BC001606.1 | AAH01606.1 | |||
| BT007439.1 | AAP36107.1 | |||
| KU178216.1 | ||||
| KU178217.1 | ||||
| M32011.1 | AAA36379.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv825587 | Chr.1:183564002 - 183573526 on Build GRCh38 | Loss |
 NCF2
|
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Set Membership: |
Intragenic
Intronic
Non-exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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