Assay Details
Target Gene Details
Entrez Gene ID: | 115286 |
Gene Name: | solute carrier family 25 member 26 |
Gene Aliases: |
COXPD28, SAMC |
Location: |
Chr.3:66133610-66380021 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
SLC25A26 | NM_173471.3 | NP_775742.4 | ||
AK092495.1 | ||||
AX747571.1 | ||||
DA845619.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv590546 | Chr.3:65487766 - 67232113 on Build GRCh38 | Gain | MAGI1 MAGI1-AS1 KBTBD8 LRIG1 SLC25A26 LOC105377143 MIR4272 |
esv3568827 | Chr.3:66138410 - 66140587 on Build GRCh38 | Loss | SLC25A26 |
More Information
Additional Information:
For this assay, SNP(s) [rs78285192] 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 Intronic Non-exonic DGV Variation |