Genomic Map
Back To TopAssay Details
Target Gene Details
Entrez Gene ID: | 641 |
Gene Name: | Bloom syndrome RecQ like helicase |
Gene Aliases: |
BS, RECQ2, RECQL2, RECQL3 |
Location: |
Chr.15:90717327-90815462 on Build GRCh38 |
Assay Gene Location: | Within Exon 4 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| BLM | NM_000057.3 | 3 | 406 | NP_000048.1 |
| NM_001287246.1 | 4 | 516 | NP_001274175.1 | |
| NM_001287247.1 | 3 | 406 | NP_001274176.1 | |
| NM_001287248.1 | 3 | 406 | NP_001274177.1 | |
| XM_011521882.2 | 3 | 393 | XP_011520184.1 | |
| AK314262.1 | 3 | 335 | ||
| BC093622.1 | 3 | 329 | AAH93622.1 | |
| BC101567.1 | 3 | 329 | AAI01568.1 | |
| BC107423.1 | 3 | 349 | AAI07424.1 | |
| BC115030.1 | 3 | 354 | AAI15031.1 | |
| BC115032.1 | 3 | 354 | AAI15033.1 | |
| BC143280.1 | 3 | 329 | ||
| BP363946.1 | 3 | 399 | ||
| CD707743.1 | 3 | 426 | ||
| U39817.1 | 3 | 362 | AAA87850.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv1045042 | Chr.15:90453811 - 90841192 on Build GRCh38 | Gain |
 CRTC3-AS1
CRTC3
IQGAP1
BLM
LINC01585
|
Back To TopMore Information
Set Membership: |
Intragenic
Exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
Back To Top