Assay Details
Target Gene Details
Entrez Gene ID: | 92105 |
Gene Name: | integrator complex subunit 4 |
Gene Aliases: |
INT4, MST093 |
Location: |
Chr.11:77874491-77994849 on Build GRCh38 |
Assay Gene Location: | Within Intron 17 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| INTS4 | NM_033547.3 | NP_291025.3 | ||
| XM_011545352.2 | XP_011543654.1 | |||
| XM_017018560.1 | XP_016874049.1 | |||
| AF172822.1 | AAQ13616.1 | |||
| AK290866.1 | ||||
| AL834171.1 | ||||
| BC006369.1 | AAH06369.1 | |||
| BC008013.1 | AAH08013.1 | |||
| BC009859.2 | AAH09859.2 | |||
| BC015664.2 | AAH15664.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv520740 | Chr.11:77842592 - 78286890 on Build GRCh38 | Gain |
|
| nsv1050891 | Chr.11:77705600 - 78076956 on Build GRCh38 | Gain |
|
More Information
Additional Information:
For this assay, SNP(s) [rs116140150] 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