Assay Details
Target Gene Details
Entrez Gene ID: | 84889 |
Gene Name: | solute carrier family 7 member 3 |
Gene Aliases: |
ATRC3, CAT-3, CAT3 |
Location: |
Chr.X:70925579-70931125 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 3 - Exon 4 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
SLC7A3 | NM_001048164.2 | NP_001041629.1 | ||
NM_032803.5 | NP_116192.4 | |||
XM_017029912.1 | XP_016885401.1 | |||
AF320612.1 | AAL37184.1 | |||
AK027447.1 | BAB55118.1 | |||
AK074865.1 | BAC11253.1 | |||
AK075014.1 | BAC11353.1 | |||
BC033816.1 | AAH33816.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv33082 | Chr.X:70420685 - 71888183 on Build GRCh38 | Loss | ACRC SLC7A3 CXorf49 SNX12 NLGN3 OGT LOC105373244 TEX11 GJB1 CXorf49B ZMYM3 LOC101059915 LOC100129291 CXCR3 NONO TAF1 MED12 LOC100132741 IL2RG GDPD2 INGX DLG3-AS1 CXorf65 DLG3 KIF4A FOXO4 LINC00891 ITGB1BP2 |
More Information
Additional Information:
For this assay, SNP(s) [rs67961679] 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 Non-exonic DGV Variation |