Genomic Map
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Target Gene Details
Entrez Gene ID: | 112399 |
Gene Name: | egl-9 family hypoxia inducible factor 3 |
Gene Aliases: |
HIFP4H3, HIFPH3, PHD3 |
Location: |
Chr.14:33924215-33951078 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| EGLN3 | NM_001308103.1 | NP_001295032.1 | ||
| NM_022073.3 | NP_071356.1 | |||
| AJ310545.1 | CAC42511.1 | |||
| AK025273.1 | BAB15101.1 | |||
| AK123350.1 | ||||
| AK225473.1 | ||||
| BC010992.2 | ||||
| BC064924.1 | ||||
| BC102030.1 | AAI02031.1 | |||
| BC105938.1 | AAI05939.1 | |||
| BC105939.1 | AAI05940.1 | |||
| BC111057.1 | ||||
| BG716229.1 | ||||
| DQ975379.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv1070213 | Chr.14:33930300 - 33936238 on Build GRCh38 | Deletion |
 EGLN3
|
| nsv1036996 | Chr.14:33834296 - 34189902 on Build GRCh38 | Gain |
EGLN3-AS1
EGLN3
|
| esv34070 | Chr.14:33763566 - 34160397 on Build GRCh38 | Loss |
NPAS3
EGLN3-AS1
EGLN3
|
| nsv832768 | Chr.14:33887269 - 34082696 on Build GRCh38 | Gain |
EGLN3-AS1
EGLN3
|
| nsv832769 | Chr.14:33927540 - 34114539 on Build GRCh38 | Loss |
EGLN3-AS1
EGLN3
|
Back To TopMore Information
Set Membership: |
Intragenic
Intronic
Non-exonic
DGV Variation
|
Gene Ontology Categories:
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