Assay Details
Target Gene Details
Entrez Gene ID: | 1829 |
Gene Name: | desmoglein 2 |
Gene Aliases: |
CDHF5, HDGC |
Location: |
Chr.18:31498004-31549008 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
DSG2 | NM_001943.4 | NP_001934.2 | ||
AK308408.1 | ||||
BC099655.3 | AAH99655.1 | |||
BC099656.3 | AAH99656.1 | |||
BC099657.3 | AAH99657.1 | |||
BP353513.1 | ||||
CN347023.1 | ||||
DC417739.1 | ||||
HY268349.1 | ||||
Z26317.1 | CAA81226.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv833615 | Chr.18:31428433 - 31613013 on Build GRCh38 | Gain | DSG2 DSG3 DSG2-AS1 TTR |
More Information
Additional Information:
For this assay, SNP(s) [rs78722216] 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 |