Assay Details
Target Gene Details
Entrez Gene ID: | 10587 |
Gene Name: | thioredoxin reductase 2 |
Gene Aliases: |
SELZ, TR, TR-BETA, TR3, TRXR2 |
Location: |
Chr.22:19875518-19941992 on Build GRCh38 |
Assay Gene Location: | Within Intron 18 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
TXNRD2 | NM_006440.4 | NP_006431.2 | ||
AB019694.1 | BAA77601.2 | |||
AB019695.1 | BAA77602.2 | |||
AB209724.1 | BAD92961.1 | |||
AF044212.1 | AAD25167.1 | |||
AF106697.1 | AAD19597.1 | |||
AF166126.1 | AAF21431.1 | |||
AF166127.1 | AAF21432.1 | |||
AF171054.1 | AAD51324.1 | |||
AF201385.1 | 17 | 2142 | AAG47635.1 | |
AK094698.1 | 5 | 1689 | ||
AK097708.1 | ||||
BC007489.2 | AAH07489.3 | |||
BC117354.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv834129 | Chr.22:19705617 - 19919068 on Build GRCh38 | Loss |
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esv3893434 | Chr.22:19470889 - 20343372 on Build GRCh38 | Gain |
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nsv828939 | Chr.22:19696032 - 20324465 on Build GRCh38 | Loss |
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nsv828938 | Chr.22:19691069 - 20324465 on Build GRCh38 | Gain |
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nsv515664 | Chr.22:19873352 - 19892114 on Build GRCh38 | Loss |
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nsv834130 | Chr.22:19837923 - 19940567 on Build GRCh38 | Loss |
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esv3568260 | Chr.22:19777375 - 19881883 on Build GRCh38 | Loss |
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esv3647279 | Chr.22:19719848 - 19878980 on Build GRCh38 | Gain |
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nsv953025 | Chr.22:19869078 - 19937977 on Build GRCh38 | Deletion |
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dgv7983n54 | Chr.22:19762002 - 20321870 on Build GRCh38 | Gain |
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esv3575418 | Chr.22:18161776 - 19963846 on Build GRCh38 | Gain |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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More Information
Additional Information:
For this assay, SNP(s) [rs73877383] 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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Panther Classification:
Gene Ontology Categories:
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