Assay Details
Target Gene Details
Entrez Gene ID: | 284427 |
Gene Name: | solute carrier family 25 member 41 |
Gene Aliases: |
APC4 |
Location: |
Chr.19:6426037-6436267 on Build GRCh38 |
Assay Gene Location: | Within Exon 9 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
SLC25A41 | NM_001321298.1 | 8 | 1279 | NP_001308227.1 |
NM_173637.3 | 7 | 1181 | NP_775908.2 | |
NR_135612.1 | 7 | 1181 | ||
XM_011527926.1 | 7 | 975 | XP_011526228.1 | |
AK097761.1 | 8 | 1263 | BAC05163.1 | |
BC031671.1 | 7 | 1181 | AAH31671.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv833727 | Chr.19:6400101 - 6568241 on Build GRCh38 | Loss | DENND1C MIR3940 KHSRP SLC25A23 SLC25A41 LOC390877 CRB3 TUBB4A TNFSF9 |
More Information
Additional Information:
For this assay, SNP(s) [rs75384914] 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 |