Genomic Map
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Target Gene Details
Entrez Gene ID: | 8678 |
Gene Name: | beclin 1 |
Gene Aliases: |
ATG6, VPS30, beclin1 |
Location: |
Chr.17:42810132-42824316 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 9 - Exon 10 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| BECN1 | NM_001313998.1 | NP_001300927.1 | ||
| NM_001313999.1 | NP_001300928.1 | |||
| NM_001314000.1 | NP_001300929.1 | |||
| NM_003766.4 | NP_003757.1 | |||
| XM_005257759.2 | XP_005257816.1 | |||
| XM_005257760.3 | XP_005257817.1 | |||
| XM_011525421.2 | XP_011523723.1 | |||
| XM_017025262.1 | XP_016880751.1 | |||
| XM_017025263.1 | XP_016880752.1 | |||
| XM_017025264.1 | XP_016880753.1 | |||
| AF077301.1 | AAC68653.1 | |||
| AF139131.1 | AAD27650.1 | |||
| AK223411.1 | BAD97131.1 | |||
| AK298619.1 | ||||
| AK299616.1 | ||||
| AK312651.1 | ||||
| BC010276.1 | AAH10276.1 | |||
| BX647788.1 | 7 | 2413 | ||
| KC776730.1 | ||||
| L38932.1 | AAB59573.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv833450 | Chr.17:42660985 - 42825144 on Build GRCh38 | Loss |
 RAMP2-AS1
TUBG2
BECN1
MIR6781
MIR6780A
COA3
PLEKHH3
EZH1
CCR10
VPS25
RAMP2
CNTNAP1
CNTD1
WNK4
|
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Set Membership: |
Intragenic
Non-exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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