Assay Details
Target Gene Details
Entrez Gene ID: | 81894 |
Gene Name: | solute carrier family 25 member 28 |
Gene Aliases: |
MFRN2, MRS3/4, MRS4L, NPD016 |
Location: |
Chr.10:99610518-99659329 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
SLC25A28 | XM_006718005.3 | XP_006718068.1 | ||
XM_017016742.1 | XP_016872231.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv7515 | Chr.10:99606658 - 99639439 on Build GRCh38 | Insertion | SLC25A28 |
nsv831958 | Chr.10:99451304 - 99651424 on Build GRCh38 | Gain | NKX2-3 LINC01475 SLC25A28 |
More Information
Additional Information:
For this assay, SNP(s) [rs78672893] 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 |