Genomic Map
Back To TopAssay Details
Target Gene Details
Entrez Gene ID: | 27242 |
Gene Name: | TNF receptor superfamily member 21 |
Gene Aliases: |
BM-018, CD358, DR6 |
Location: |
Chr.6:47231527-47309976 on Build GRCh38 |
Assay Gene Location: | Within Exon 7 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| TNFRSF21 | NM_014452.4 | 6 | 2645 | NP_055267.1 |
| AB209394.1 | 5 | 3836 | BAD92631.1 | |
| AJ420531.1 | 5 | 2014 | ||
| AK001504.1 | ||||
| AY358304.1 | 6 | 2533 | AAQ88671.1 | |
| BC010241.1 | 5 | 1802 | AAH10241.1 | |
| BC017730.2 | 6 | 2220 | AAH17730.1 | |
| BC021572.1 | 6 | 2521 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv1017113 | Chr.6:46846140 - 48020279 on Build GRCh38 | Gain |
 ADGRF4
ADGRF2
ADGRF5
LOC101926962
ADGRF1
PTCHD4
CD2AP
OPN5
TNFRSF21
|
Back To TopMore Information
Additional Information:
For this assay, SNP(s) [rs112278570] 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
|
Panther Classification:
Gene Ontology Categories:
Back To Top