Genomic Map
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Target Gene Details
Entrez Gene ID: | 9774 |
Gene Name: | BCL2 associated transcription factor 1 |
Gene Aliases: |
BTF, bK211L9.1 |
Location: |
Chr.6:136256863-136290645 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 13 - Exon 14 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| BCLAF1 | NM_001077440.1 | NP_001070908.1 | ||
| NM_001077441.1 | NP_001070909.1 | |||
| NM_001301038.1 | NP_001287967.1 | |||
| NM_014739.2 | NP_055554.1 | |||
| XM_005267237.3 | XP_005267294.1 | |||
| XM_017011529.1 | XP_016867018.1 | |||
| XM_017011530.1 | XP_016867019.1 | |||
| XM_017011531.1 | XP_016867020.1 | |||
| XM_017011532.1 | XP_016867021.1 | |||
| AK303559.1 | ||||
| AK308870.1 | ||||
| AK315884.1 | ||||
| BC132780.1 | ||||
| BC144281.1 | ||||
| BX537576.1 | 1 | 2204 | ||
| BX648431.1 | ||||
| BX648878.1 | ||||
| BX649160.1 | ||||
| D79986.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv3540516 | Chr.6:136261081 - 136269403 on Build GRCh38 | Deletion |
 BCLAF1
|
| esv9082 | Chr.6:136261072 - 136268342 on Build GRCh38 | Loss |
BCLAF1
|
| nsv1074963 | Chr.6:136261061 - 136261272 on Build GRCh38 | Deletion |
BCLAF1
|
| nsv1121355 | Chr.6:136261064 - 136261263 on Build GRCh38 | Deletion |
BCLAF1
|
| nsv955912 | Chr.6:136261099 - 136261255 on Build GRCh38 | Deletion |
BCLAF1
|
| esv2732746 | Chr.6:136261057 - 136261279 on Build GRCh38 | Deletion |
BCLAF1
|
| nsv1111702 | Chr.6:136261158 - 136261277 on Build GRCh38 | Deletion |
BCLAF1
|
Back To TopMore Information
Set Membership: |
Intragenic
Non-exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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