Assay Details
Target Gene Details
Entrez Gene ID: | 10732 |
Gene Name: | transcription factor like 5 |
Gene Aliases: |
CHA, E2BP-1, Figlb, bHLHe82 |
Location: |
Chr.20:62841014-62861763 on Build GRCh38 |
Assay Gene Location: | Within Intron 6 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| TCFL5 | NM_006602.3 | NP_006593.2 | ||
| XM_005260185.3 | XP_005260242.1 | |||
| XM_011528497.2 | XP_011526799.1 | |||
| XM_011528499.1 | XP_011526801.1 | |||
| AB012124.1 | BAA36557.1 | |||
| AF070992.1 | AAD53986.1 | |||
| AJ271337.1 | CAC24700.1 | |||
| BC046933.1 | AAH46933.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv834027 | Chr.20:62707655 - 62874914 on Build GRCh38 | Loss |
|
| nsv828794 | Chr.20:62832958 - 62880035 on Build GRCh38 | Loss |
|
| nsv9825 | Chr.20:62775470 - 63601330 on Build GRCh38 | Gain |
|
| nsv428380 | Chr.20:62632018 - 62935383 on Build GRCh38 | Loss |
|
More Information
Additional Information:
For this assay, SNP(s) [rs66634465] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Set Membership: |
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Genomic Map