Assay Details
Target Gene Details
Entrez Gene ID: | 116028 |
Gene Name: | RecQ mediated genome instability 2 |
Gene Aliases: |
BLAP18, C16orf75 |
Location: |
Chr.16:11345438-11351763 on Build GRCh38 |
Assay Gene Location: | Within Exon 2 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
RMI2 | NM_152308.2 | 2 | 947 | NP_689521.1 |
NR_130754.1 | 2 | 724 | ||
AK123764.1 | 2 | 936 | ||
BC013040.2 | 2 | 915 | AAH13040.2 | |
BC022427.1 | 2 | 931 | AAH22427.1 | |
BC031016.1 | 2 | 935 | AAH31016.1 | |
BC039361.1 | 5 | 1369 | AAH39361.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
dgv2728n100 | Chr.16:11333115 - 11449038 on Build GRCh38 | Gain |
![]() ![]() ![]() |
nsv1040428 | Chr.16:10145408 - 11362136 on Build GRCh38 | Gain |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)
More Information
Additional Information:
For this assay, SNP(s) [rs75818242] 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: |
![]() ![]() ![]() |
Gene Ontology Categories:
![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)