Genomic Map
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Target Gene Details
Entrez Gene ID: | 6939 |
Gene Name: | transcription factor 15 (basic helix-loop-helix) |
Gene Aliases: |
EC2, PARAXIS, bHLHa40 |
Location: |
Chr.20:603993-610266 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| TCF15 | NM_004609.3 | NP_004600.2 | ||
| AI218364.1 | ||||
| AW290965.1 | ||||
| BC067836.1 | AAH67836.1 | |||
| U08336.1 | AAA19969.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv1058681 | Chr.20:567543 - 606311 on Build GRCh38 | Loss |
 TCF15
|
| nsv585173 | Chr.20:592392 - 625245 on Build GRCh38 | Loss |
TCF15
|
| nsv469833 | Chr.20:447851 - 614798 on Build GRCh38 | Gain |
TBC1D20
TCF15
CSNK2A1
|
| esv3644952 | Chr.20:386013 - 1119183 on Build GRCh38 | Gain |
RSPO4
SRXN1
TRIB3
LOC105372493
FAM110A
CSNK2A1
TBC1D20
PSMF1
SLC52A3
RBCK1
TCF15
SCRT2
ANGPT4
|
| nsv458845 | Chr.20:602943 - 625293 on Build GRCh38 | Loss |
TCF15
|
| nsv833891 | Chr.20:468248 - 620062 on Build GRCh38 | Gain+Loss |
TCF15
CSNK2A1
|
| nsv458844 | Chr.20:599013 - 614136 on Build GRCh38 | Loss |
TCF15
|
| nsv585172 | Chr.20:551334 - 613017 on Build GRCh38 | Gain |
TCF15
|
Back To TopMore Information
Set Membership: |
Intragenic
Intronic
Non-exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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