Genomic Map
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Target Gene Details
Entrez Gene ID: | 4779 |
Gene Name: | nuclear factor, erythroid 2 like 1 |
Gene Aliases: |
LCR-F1, NRF1, TCF11 |
Location: |
Chr.17:48048324-48061545 on Build GRCh38 |
Assay Gene Location: | Within Exon 3 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| NFE2L1 | NM_003204.2 | 2 | 1100 | NP_003195.1 |
| XM_005257410.3 | 2 | 1046 | XP_005257467.1 | |
| XM_005257411.3 | 2 | 1046 | XP_005257468.1 | |
| XM_005257412.3 | 2 | 1046 | XP_005257469.1 | |
| XM_005257413.3 | 2 | 1100 | XP_005257470.1 | |
| XM_005257415.3 | 2 | 1046 | XP_005257472.1 | |
| XM_017024691.1 | 2 | 1100 | XP_016880180.1 | |
| AK090459.1 | 2 | 1065 | ||
| AL833530.1 | 3 | 765 | ||
| BC010623.1 | 2 | 1082 | AAH10623.1 | |
| BC131769.1 | 1 | 693 | ||
| BX647976.1 | 2 | 1054 | ||
| L24123.1 | 2 | 1378 | ||
| X77366.1 | 2 | 1040 | CAA54555.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv469808 | Chr.17:47972502 - 48151311 on Build GRCh38 | Loss |
 CBX1
SKAP1
NFE2L1
COPZ2
MIR152
CDK5RAP3
SNX11
|
| nsv953920 | Chr.17:48049839 - 48062838 on Build GRCh38 | Deletion |
NFE2L1
|
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Set Membership: |
Intragenic
Exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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