Assay Details
Target Gene Details
Entrez Gene ID: | 4600 |
Gene Name: | MX dynamin like GTPase 2 |
Gene Aliases: |
MXB |
Location: |
Chr.21:41361986-41408943 on Build GRCh38 |
Assay Gene Location: | Within Intron 5 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
MX2 | NM_002463.1 | NP_002454.1 | ||
XM_005260983.4 | XP_005261040.1 | |||
XM_005260984.1 | XP_005261041.1 | |||
XM_011529571.1 | XP_011527873.1 | |||
XM_011529572.1 | XP_011527874.1 | |||
XM_011529573.1 | XP_011527875.1 | |||
AK298780.1 | ||||
AK308060.1 | ||||
M30818.1 | AAA36338.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv528279 | Chr.21:41357910 - 41380411 on Build GRCh38 | Gain |
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nsv834102 | Chr.21:41286267 - 41494006 on Build GRCh38 | Loss |
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dgv7834n54 | Chr.21:41369022 - 41395967 on Build GRCh38 | Loss |
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nsv1057981 | Chr.21:41290295 - 41422831 on Build GRCh38 | Loss |
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esv3647060 | Chr.21:41349724 - 41420569 on Build GRCh38 | Gain |
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esv3647061 | Chr.21:41354348 - 41391162 on Build GRCh38 | Gain |
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![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)
More Information
Additional Information:
For this assay, SNP(s) [rs72301630] 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:
![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)