Assay Details
Target Gene Details
Entrez Gene ID: | 100526693 |
Gene Name: | ARPC4-TTLL3 readthrough |
Gene Aliases: |
- |
Location: |
Chr.3:9792548-9836356 on Build GRCh38 |
Assay Gene Location: | Within Intron 4 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
ARPC4-TTLL3 | NM_001198793.1 | NP_001185722.1 | ||
AK024110.1 | BAB14828.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1010768 | Chr.3:9502870 - 9873902 on Build GRCh38 | Gain | LHFPL4 TADA3 CIDEC RPUSD3 BRPF1 OGG1 LOC107986062 MTMR14 TTLL3 CPNE9 ARPC4-TTLL3 ARPC4 CAMK1 |
nsv834615 | Chr.3:9791053 - 9971639 on Build GRCh38 | Loss | TADA3 CIDEC RPUSD3 LOC107986062 CRELD1 IL17RE TTLL3 PRRT3-AS1 EMC3 ARPC4-TTLL3 PRRT3 JAGN1 ARPC4 IL17RC |
More Information
Additional Information:
For this assay, SNP(s) [rs73811573] 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: |
Intragenic Intronic Non-exonic DGV Variation |