Assay Details
Target Gene Details
Entrez Gene ID: | 23101 |
Gene Name: | MCF.2 cell line derived transforming sequence-like 2 |
Gene Aliases: |
ARHGEF22 |
Location: |
Chr.3:183176116-183428990 on Build GRCh38 |
Assay Gene Location: | Within Intron 24 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| MCF2L2 | NM_015078.3 | NP_055893.3 | ||
| XM_011512585.2 | XP_011510887.1 | |||
| XM_011512586.2 | XP_011510888.1 | |||
| XM_017005943.1 | XP_016861432.1 | |||
| AB020668.1 | BAA74884.1 | |||
| AY172737.1 | AAO19651.1 | |||
| BC029074.2 | AAH29074.2 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv3893833 | Chr.3:183130677 - 183342208 on Build GRCh38 | Gain |
|
| nsv1006872 | Chr.3:183194738 - 183548501 on Build GRCh38 | Loss |
|
More Information
Additional Information:
For this assay, SNP(s) [rs75677427] 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: |
|

Genomic Map