Assay Details
Target Gene Details
Entrez Gene ID: | 11033 |
Gene Name: | ArfGAP with dual PH domains 1 |
Gene Aliases: |
CENTA1, GCS1L, p42IP4 |
Location: |
Chr.7:897900-955407 on Build GRCh38 |
Assay Gene Location: | Within Intron 8 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| ADAP1 | NM_001284308.1 | NP_001271237.1 | ||
| NM_001284309.1 | NP_001271238.1 | |||
| NM_001284310.1 | NP_001271239.1 | |||
| NM_001284311.1 | NP_001271240.1 | |||
| NM_006869.3 | NP_006860.1 | |||
| AB097049.1 | BAC77402.1 | |||
| AF082324.1 | AAD11414.1 | |||
| AJ006422.1 | CAA07024.1 | |||
| AK092471.1 | ||||
| AK290517.1 | ||||
| AK300644.1 | ||||
| AK300859.1 | ||||
| AK300999.1 | ||||
| BC033747.1 | AAH33747.1 | |||
| BM837987.1 | ||||
| DA872042.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv605700 | Chr.7:886440 - 1065790 on Build GRCh38 | Gain |
|
| esv3611796 | Chr.7:904223 - 922273 on Build GRCh38 | Gain |
|
| nsv605699 | Chr.7:886312 - 1073232 on Build GRCh38 | Loss |
|
| nsv509182 | Chr.7:881218 - 1018010 on Build GRCh38 | Insertion |
|
| nsv605702 | Chr.7:890175 - 947983 on Build GRCh38 | Loss |
|
| nsv950784 | Chr.7:855964 - 1074664 on Build GRCh38 | Deletion |
|
| esv3571557 | Chr.7:823644 - 994725 on Build GRCh38 | Loss |
|
| dgv11111n54 | Chr.7:873118 - 983092 on Build GRCh38 | Loss |
|
More Information
Additional Information:
For this assay, SNP(s) [rs114350402] 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