Assay Details
Target Gene Details
Entrez Gene ID: | 10322 |
Gene Name: | SMYD family member 5 |
Gene Aliases: |
NN8-4AG, RAI15, RRG1, ZMYND23 |
Location: |
Chr.2:73214238-73227227 on Build GRCh38 |
Assay Gene Location: | Within Exon 13 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
SMYD5 | NM_006062.2 | 13 | 1515 | NP_006053.2 |
XM_006711918.3 | 13 | 1602 | XP_006711981.1 | |
XM_017003163.1 | 12 | 3235 | XP_016858652.1 | |
AK300779.1 | ||||
AK301809.1 | ||||
BC073806.1 | 13 | 1491 | AAH73806.1 | |
U50383.1 | 13 | 1468 | AAB38131.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv2776 | Chr.2:73204726 - 73255176 on Build GRCh38 | Deletion | FBXO41 SMYD5 NOTO PRADC1 CCT7 |
More Information
Additional Information:
For this assay, SNP(s) [rs74567063] 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 |