Assay Details
Target Gene Details
Entrez Gene ID: | 373 |
Gene Name: | tripartite motif containing 23 |
Gene Aliases: |
ARD1, ARFD1, RNF46 |
Location: |
Chr.5:65589680-65624360 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 10 - Exon 11 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| TRIM23 | NM_001656.3 | NP_001647.1 | ||
| NM_033227.2 | NP_150230.1 | |||
| NM_033228.2 | NP_150231.1 | |||
| XM_005248497.3 | XP_005248554.1 | |||
| XM_017009444.1 | XP_016864933.1 | |||
| AF230397.1 | AAG50176.1 | |||
| AF230398.1 | AAG50177.1 | |||
| AF230399.1 | AAG50178.1 | |||
| AK292814.1 | ||||
| BC022510.1 | AAH22510.1 | |||
| L04510.1 | AAA35940.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv3894204 | Chr.5:65586109 - 65714937 on Build GRCh38 | Loss |
|
More Information
Additional Information:
For this assay, SNP(s) [rs200591165] 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: |
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Genomic Map