Assay Details
Target Gene Details
Entrez Gene ID: | 389668 |
Gene Name: | XK related 9 |
Gene Aliases: |
XRG9 |
Location: |
Chr.8:70669365-71066635 on Build GRCh38 |
Assay Gene Location: | Within Exon 11 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| XKR9 | NM_001011720.1 | 5 | 1884 | NP_001011720.1 |
| NM_001287258.1 | 6 | 2002 | NP_001274187.1 | |
| NM_001287259.1 | 6 | 1994 | NP_001274188.1 | |
| NM_001287260.1 | 5 | 1738 | NP_001274189.1 | |
| XM_011517527.2 | XP_011515829.1 | |||
| AY534247.1 | 5 | 1884 | AAT07096.1 | |
| BC137104.1 | ||||
| BC137105.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv3576585 | Chr.8:70645369 - 70750875 on Build GRCh38 | Gain |
|
More Information
Additional Information:
For this assay, SNP(s) [rs199532081] 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