Assay Details
Target Gene Details
Entrez Gene ID: | 399664 |
Gene Name: | mex-3 RNA binding family member D |
Gene Aliases: |
MEX-3D, MEX3, OK/SW-cl.4, RKHD1, RNF193, TINO |
Location: |
Chr.19:1554669-1568058 on Build GRCh38 |
Assay Gene Location: | Within Exon 3 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| MEX3D | NM_001174118.1 | 3 | 2131 | NP_001167589.1 |
| NM_203304.3 | 2 | 2318 | NP_976049.3 | |
| XM_017026811.1 | 2 | 2118 | XP_016882300.1 | |
| AB062435.1 | 1 | 331 | BAB93498.1 | |
| AB107353.1 | 2 | 1911 | BAC67658.1 | |
| AF458084.1 | 3 | 1603 | AAQ04763.1 | |
| BC113384.1 | ||||
| BC113741.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv32942 | Chr.19:1320268 - 1999205 on Build GRCh38 | Gain+Loss |
|
| nsv1121962 | Chr.19:1554801 - 1555701 on Build GRCh38 | Deletion |
|
| nsv517758 | Chr.19:1550651 - 1572370 on Build GRCh38 | Loss |
|
| nsv1072837 | Chr.19:1554900 - 1555701 on Build GRCh38 | Deletion |
|
| nsv953942 | Chr.19:1371602 - 2057401 on Build GRCh38 | Deletion |
|
More Information
Additional Information:
For this assay, SNP(s) [rs182474457] 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