Assay Details
Target Gene Details
Entrez Gene ID: | 23539 |
Gene Name: | solute carrier family 16 member 8 |
Gene Aliases: |
MCT3, REMP |
Location: |
Chr.22:38078137-38083163 on Build GRCh38 |
Assay Gene Location: | Within Exon 3 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
SLC16A8 | NM_013356.2 | 4 | 922 | NP_037488.2 |
XM_017028685.1 | 3 | 977 | XP_016884174.1 | |
AF132610.1 | 4 | 901 | AAF03565.1 | |
BM714896.1 | 2 | 501 | ||
BM714916.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv527871 | Chr.22:38078689 - 38084652 on Build GRCh38 | Loss | SLC16A8 |
nsv471198 | Chr.22:38019714 - 38149612 on Build GRCh38 | Loss | PLA2G6 POLR2F BAIAP2L2 PICK1 SLC16A8 |
nsv834194 | Chr.22:38063495 - 38240504 on Build GRCh38 | Loss | SNORA92 PLA2G6 TMEM184B BAIAP2L2 MAFF PICK1 SLC16A8 |
nsv834193 | Chr.22:37997329 - 38172090 on Build GRCh38 | Loss | PLA2G6 POLR2F BAIAP2L2 PICK1 SLC16A8 |
More Information
Additional Information:
For this assay, SNP(s) [rs75640043] 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: |
Intragenic Exonic DGV Variation |