Assay Details
Target Gene Details
Entrez Gene ID: | 8120 |
Gene Name: | adaptor related protein complex 3 beta 2 subunit |
Gene Aliases: |
NAPTB |
Location: |
Chr.15:82659281-82710112 on Build GRCh38 |
Assay Gene Location: | Overlaps - Exon 28 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
AP3B2 | NM_001278511.1 | NP_001265440.1 | ||
NM_001278512.1 | NP_001265441.1 | |||
NM_004644.4 | NP_004635.2 | |||
XM_017022640.1 | XP_016878129.1 | |||
AF022152.1 | AAB71894.1 | |||
AK097827.1 | ||||
CR749860.1 | CAH18704.2 | |||
DQ092369.1 |
Target Gene Details
Entrez Gene ID: | 283692 |
Gene Name: | CPEB1 antisense RNA 1 |
Gene Aliases: |
- |
Location: |
Chr.15:82647770-82692820 on Build GRCh38 |
Assay Gene Location: | Within Intron 3 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
CPEB1-AS1 | NR_046096.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv3637058 | Chr.15:82590287 - 82726611 on Build GRCh38 | Gain | CPEB1 LOC338963 CPEB1-AS1 AP3B2 ACTG1P17 |
dgv2637n100 | Chr.15:82568764 - 82803755 on Build GRCh38 | Gain | CPEB1 LOC338963 CPEB1-AS1 SCARNA15 AP3B2 ACTG1P17 FSD2 SNHG21 |
nsv817702 | Chr.15:82630710 - 82788672 on Build GRCh38 | Loss | CPEB1 LOC338963 CPEB1-AS1 SCARNA15 AP3B2 ACTG1P17 FSD2 SNHG21 |
esv23134 | Chr.15:82658385 - 82663620 on Build GRCh38 | Gain | CPEB1-AS1 AP3B2 |
esv34318 | Chr.15:82614804 - 82784743 on Build GRCh38 | Loss | CPEB1 LOC338963 CPEB1-AS1 SCARNA15 AP3B2 ACTG1P17 FSD2 SNHG21 |
esv2674021 | Chr.15:82628241 - 82789040 on Build GRCh38 | Deletion | CPEB1 LOC338963 CPEB1-AS1 SCARNA15 AP3B2 ACTG1P17 FSD2 SNHG21 |
More Information
Additional Information:
For this assay, SNP(s) [rs77082021] 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 |