Assay Details
Target Gene Details
Entrez Gene ID: | 84250 |
Gene Name: | SMC5-SMC6 complex localization factor 1 |
Gene Aliases: |
ANKRD32, BRCTD1, BRCTx |
Location: |
Chr.5:94613477-94697733 on Build GRCh38 |
Assay Gene Location: | Within Intron 7 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| SLF1 | NM_032290.3 | NP_115666.2 | ||
| XM_017009978.1 | XP_016865467.1 | |||
| XM_017009979.1 | XP_016865468.1 | |||
| XM_017009980.1 | XP_016865469.1 | |||
| XM_017009981.1 | XP_016865470.1 | |||
| XM_017009982.1 | XP_016865471.1 | |||
| AK297452.1 | ||||
| AK299080.1 | ||||
| AL050298.1 | CAB43397.2 | |||
| BC054885.1 | AAH54885.2 | |||
| BC070332.1 | AAH70332.1 | |||
| BC107571.1 | AAI07572.1 | |||
| BU431750.1 | ||||
| CR936768.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv435825 | Chr.5:94642472 - 94648809 on Build GRCh38 | Deletion |
|
| nsv462254 | Chr.5:94621232 - 94721120 on Build GRCh38 | Loss |
|
| esv2759354 | Chr.5:94429500 - 94706496 on Build GRCh38 | Loss |
|
More Information
Additional Information:
For this assay, SNP(s) [rs79372314] 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: |
|

Genomic Map