Genomic Map
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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 14 |
| 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 | |||
| Z26317.1 | CAA81226.1 |
Target Gene Details
Entrez Gene ID: | 100652770 |
Gene Name: | DSG2 antisense RNA 1 |
Gene Aliases: |
- |
Location: |
Chr.18:31542146-31556911 on Build GRCh38 |
Assay Gene Location: | Within Intron 4 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| DSG2-AS1 | NR_045216.1 |
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 |
 DSG3
DSG2
DSG2-AS1
TTR
|
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Additional Information:
For this assay, SNP(s) [rs112696044] 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
|
Panther Classification:
Gene Ontology Categories:
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