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: | Within Exon 14 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
AP3B2 | NM_001278511.1 | 13 | 1698 | NP_001265440.1 |
NM_001278512.1 | 14 | 1794 | NP_001265441.1 | |
NM_004644.4 | 14 | 1794 | NP_004635.2 | |
XM_017022640.1 | 13 | 1926 | XP_016878129.1 | |
XM_017022641.1 | 14 | 1998 | XP_016878130.1 | |
AF022152.1 | 14 | 1623 | AAB71894.1 | |
AK097827.1 | 6 | 691 | ||
BC093739.1 | 14 | 1665 | AAH93739.1 | |
BC143342.1 | 13 | 1569 | ||
BC143346.1 | 14 | 1665 | ||
CR749860.1 | 13 | 1794 | CAH18704.2 | |
U37673.1 | 14 | 1650 | AAC50219.1 |
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-AS1 CPEB1 AP3B2 LOC338963 ACTG1P17 |
dgv2637n100 | Chr.15:82568764 - 82803755 on Build GRCh38 | Gain | SNHG21 CPEB1-AS1 CPEB1 AP3B2 FSD2 SCARNA15 LOC338963 ACTG1P17 |
nsv817702 | Chr.15:82630710 - 82788672 on Build GRCh38 | Loss | SNHG21 CPEB1-AS1 CPEB1 AP3B2 FSD2 SCARNA15 LOC338963 ACTG1P17 |
esv34318 | Chr.15:82614804 - 82784743 on Build GRCh38 | Loss | SNHG21 CPEB1-AS1 CPEB1 AP3B2 FSD2 SCARNA15 LOC338963 ACTG1P17 |
esv2674021 | Chr.15:82628241 - 82789040 on Build GRCh38 | Deletion | SNHG21 CPEB1-AS1 CPEB1 AP3B2 FSD2 SCARNA15 LOC338963 ACTG1P17 |
More Information
Set Membership: |
Intragenic Exonic Intronic Non-exonic DGV Variation |