Assay Details
Target Gene Details
Entrez Gene ID: | 50651 |
Gene Name: | solute carrier family 45 member 1 |
Gene Aliases: |
DNB5 |
Location: |
Chr.1:8318085-8344167 on Build GRCh38 |
Assay Gene Location: | Within Intron 6 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
SLC45A1 | NM_001080397.2 | NP_001073866.2 | ||
XM_011541530.1 | XP_011539832.1 | |||
XM_011541531.1 | XP_011539833.1 | |||
AF118274.1 | AAD27583.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1012977 | Chr.1:8252522 - 8485210 on Build GRCh38 | Loss | SLC45A1 RERE LOC102724552 |
nsv516827 | Chr.1:8330828 - 8363450 on Build GRCh38 | Loss | SLC45A1 RERE |
nsv1743 | Chr.1:8317693 - 8351656 on Build GRCh38 | Insertion | SLC45A1 |
More Information
Additional Information:
For this assay, SNP(s) [rs78463645] 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 |