Assay Details
Target Gene Details
Entrez Gene ID: | 55698 |
Gene Name: | Rap associating with DIL domain |
Gene Aliases: |
RASIP2 |
Location: |
Chr.7:4799109-4883704 on Build GRCh38 |
Assay Gene Location: | Within Intron 12 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| RADIL | NM_018059.4 | NP_060529.4 | ||
| AB058752.1 | ||||
| AK000997.1 | BAA91459.1 | |||
| AK001186.1 | BAA91543.1 | |||
| AK294745.1 | ||||
| AK296325.1 | ||||
| AL136731.1 | CAB66665.2 | |||
| BC004919.2 | AAH04919.2 | |||
| BC117317.1 | ||||
| BC126311.1 | ||||
| BC143526.1 | ||||
| EF560723.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv605978 | Chr.7:4788446 - 4814961 on Build GRCh38 | Gain |
|
| esv3611949 | Chr.7:4780814 - 4807022 on Build GRCh38 | Loss |
|
| nsv471293 | Chr.7:4725230 - 4845590 on Build GRCh38 | Loss |
|
| nsv5626 | Chr.7:4788037 - 4819657 on Build GRCh38 | Insertion |
|
| nsv1029123 | Chr.7:4782103 - 4879646 on Build GRCh38 | Loss |
|
| esv2664593 | Chr.7:4769570 - 4811687 on Build GRCh38 | Deletion |
|
| nsv528748 | Chr.7:4780950 - 4971362 on Build GRCh38 | Loss |
|
| nsv8033 | Chr.7:4762656 - 5046966 on Build GRCh38 | Loss |
|
| nsv823994 | Chr.7:4752754 - 4888697 on Build GRCh38 | Gain |
|
| nsv950797 | Chr.7:4749070 - 4811369 on Build GRCh38 | Deletion |
|
More Information
Additional Information:
For this assay, SNP(s) [rs114084438] 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