Assay Details
Target Gene Details
Entrez Gene ID: | 170591 |
Gene Name: | S100 calcium binding protein Z |
Gene Aliases: |
Gm625, S100-zeta |
Location: |
Chr.5:76849953-76952882 on Build GRCh38 |
Assay Gene Location: | Within Exon 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
S100Z | NM_130772.3 | NP_570128.2 | ||
XM_011543239.2 | 1 | 71 | XP_011541541.1 | |
XM_011543240.2 | 1 | 71 | XP_011541542.1 | |
XM_011543241.2 | 1 | 71 | XP_011541543.1 | |
XM_011543244.2 | 1 | 69 | XP_011541546.1 | |
XM_017009173.1 | 1 | 71 | XP_016864662.1 | |
BC022320.1 | AAH22320.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv2762526 | Chr.5:76838952 - 76858109 on Build GRCh38 | Loss | S100Z |
esv3605476 | Chr.5:76841495 - 76850134 on Build GRCh38 | Loss | S100Z |
esv34133 | Chr.5:76842871 - 76943505 on Build GRCh38 | Loss | S100Z |
More Information
Additional Information:
For this assay, SNP(s) [rs114235150] 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 |