Assay Details
Target Gene Details
Entrez Gene ID: | 54797 |
Gene Name: | mediator complex subunit 18 |
Gene Aliases: |
p28b |
Location: |
Chr.1:28329002-28335967 on Build GRCh38 |
Assay Gene Location: | Overlaps Exon 3 - Intron 3 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| MED18 | NM_001127350.1 | NP_001120822.1 | ||
| NM_017638.2 | NP_060108.2 | |||
| XM_005245914.4 | XP_005245971.1 | |||
| AB107222.1 | BAD06869.1 | |||
| AK000052.1 | BAA90910.1 | |||
| AK296130.1 | ||||
| BC002694.2 | AAH02694.1 | |||
| BG752399.1 | ||||
| DA090416.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv545916 | Chr.1:28208722 - 28624350 on Build GRCh38 | Gain |
|
More Information
Additional Information:
For this assay, SNP(s) [rs76452396] 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