Assay Details
Target Gene Details
Entrez Gene ID: | 116969 |
Gene Name: | ADP-ribosyltransferase 5 |
Gene Aliases: |
ARTC5 |
Location: |
Chr.11:3638503-3642392 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 1 - Exon 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| ART5 | NM_001079536.1 | NP_001073004.1 | ||
| NM_001297668.1 | NP_001284597.1 | |||
| NM_053017.4 | NP_443750.2 | |||
| NR_123732.1 | ||||
| XM_005252779.3 | XP_005252836.1 | |||
| XM_006718136.3 | XP_006718199.1 | |||
| XM_011519879.2 | XP_011518181.1 | |||
| XM_017017171.1 | XP_016872660.1 | |||
| AK313531.1 | ||||
| AY358466.1 | AAQ88831.1 | |||
| BC014577.1 | AAH14577.1 | |||
| BI825352.1 | ||||
| CD557970.1 | ||||
| HY018364.1 | ||||
| Y16835.1 | CAC79987.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv2759796 | Chr.11:3215282 - 3780199 on Build GRCh38 | Gain+Loss |
|
| nsv526441 | Chr.11:3604947 - 3735456 on Build GRCh38 | Gain |
|
| nsv428247 | Chr.11:3595654 - 3780199 on Build GRCh38 | Loss |
|
| esv2760300 | Chr.11:3395259 - 3646758 on Build GRCh38 | Gain |
|
| nsv832051 | Chr.11:3502717 - 3707484 on Build GRCh38 | Gain |
|
| nsv8775 | Chr.11:3641782 - 3643637 on Build GRCh38 | Loss |
|
| nsv1046356 | Chr.11:3607607 - 3752985 on Build GRCh38 | Gain |
|
| esv3625147 | Chr.11:3607625 - 3732043 on Build GRCh38 | Gain |
|
| nsv509385 | Chr.11:3633958 - 3656981 on Build GRCh38 | Insertion |
|
| esv28322 | Chr.11:3404851 - 3654759 on Build GRCh38 | Gain+Loss |
|
| esv2760179 | Chr.11:3631663 - 3655866 on Build GRCh38 | Loss |
|
| esv3625148 | Chr.11:3609614 - 3680474 on Build GRCh38 | Gain |
|
More Information
Additional Information:
For this assay, SNP(s) [rs113595429,rs75902876] 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