Genomic Map
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Target Gene Details
Entrez Gene ID: | 4853 |
Gene Name: | notch 2 |
Gene Aliases: |
AGS2, HJCYS, hN2 |
Location: |
Chr.1:119911553-120073449 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 37 - Exon 37 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| NOTCH2 | NM_024408.3 | NP_077719.2 | ||
| XM_005270901.3 | XP_005270958.1 | |||
| XM_011541519.2 | XP_011539821.1 | |||
| XM_011541520.2 | XP_011539822.1 | |||
| XM_017001372.1 | XP_016856861.1 | |||
| XM_017001373.1 | XP_016856862.1 | |||
| AF308601.1 | AAA36377.2 | |||
| AF315356.1 | AAG37073.1 | |||
| AK027869.1 | BAB55419.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv2610 | Chr.1:119908437 - 119940512 on Build GRCh38 | Deletion |
 NOTCH2
|
| nsv831226 | Chr.1:119788976 - 119980845 on Build GRCh38 | Gain+Loss |
NOTCH2
REG4
ADAM30
NBPF7
|
| nsv436325 | Chr.1:119848291 - 119991491 on Build GRCh38 | Deletion |
NOTCH2
ADAM30
|
| nsv547625 | Chr.1:119880082 - 119923485 on Build GRCh38 | Loss |
NOTCH2
ADAM30
|
| nsv524681 | Chr.1:118890895 - 121570001 on Build GRCh38 | Gain |
ZNF697
HAO2
WARS2-IT1
LINC00623
LOC100996721
SRGAP2-AS1
FAM72B
SEC22B
PPIAL4A
HSD3B2
LOC101929147
HIST2H2BA
TBX15
RNVU1-19
NBPF26
LOC100996318
LOC101929798
LINC00622
NBPF7
NBPF8
NOTCH2
LOC105378933
PHGDH
LOC100996720
PFN1P2
EMBP1
ADAM30
FCGR1B
LOC101929796
HMGCS2
LOC100996724
RNVU1-4
HAO2-IT1
LOC105369199
SRGAP2C
REG4
HSD3B1
HSD3BP4
WARS2
|
| nsv428201 | Chr.1:119724690 - 120154589 on Build GRCh38 | Gain |
SEC22B
NOTCH2
HMGCS2
PHGDH
REG4
ADAM30
NBPF7
|
Back To TopMore Information
Set Membership: |
Intragenic
Non-exonic
DGV Variation
|
Gene Ontology Categories:
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