Assay Details
Target Gene Details
Entrez Gene ID: | 283652 |
Gene Name: | solute carrier family 24 member 5 |
Gene Aliases: |
JSX, NCKX5, OCA6, SHEP4 |
Location: |
Chr.15:48120972-48142392 on Build GRCh38 |
Assay Gene Location: | Within Intron 4 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
SLC24A5 | NM_205850.2 | NP_995322.1 | ||
XM_017022079.1 | XP_016877568.1 | |||
XM_017022080.1 | XP_016877569.1 | |||
AF348468.1 | AAQ15116.1 | |||
BC113628.1 | ||||
BC113630.1 | ||||
BC143950.1 | ||||
DQ665306.1 | ||||
DQ665307.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv832999 | Chr.15:47960097 - 48160208 on Build GRCh38 | Gain | SLC24A5 MYEF2 |
nsv569338 | Chr.15:48104611 - 48160602 on Build GRCh38 | Loss | SLC24A5 MYEF2 |
More Information
Additional Information:
For this assay, SNP(s) [rs115638698] 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 |