Assay Details
Target Gene Details
Entrez Gene ID: | 347 |
Gene Name: | apolipoprotein D |
Gene Aliases: |
- |
Location: |
Chr.3:195568702-195584205 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 3 - Exon 3 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
APOD | NM_001647.3 | NP_001638.1 | ||
AK294523.1 | ||||
AK312090.1 | ||||
BC007402.2 | AAH07402.1 | |||
BQ008672.1 | ||||
BT019860.1 | AAV38663.1 | |||
BT019861.1 | AAV38664.1 | |||
BU195270.1 | ||||
CR456838.1 | CAG33119.1 | |||
CR541773.1 | CAG46572.1 | |||
DA892855.1 | ||||
J02611.1 | AAB59517.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
dgv5016n100 | Chr.3:195552380 - 195720039 on Build GRCh38 | Gain+Loss | SDHAP2 MIR570 LOC105374297 APOD LINC00969 |
nsv1001387 | Chr.3:195465410 - 195934667 on Build GRCh38 | Gain | SDHAP2 LOC101929697 TNK2 LOC105374299 MUC20 MUC4 MIR570 PPP1R2 LOC105374297 APOD LINC00969 MIR6829 |
dgv5015n100 | Chr.3:195532487 - 195751823 on Build GRCh38 | Loss | SDHAP2 MUC20 MUC4 MIR570 PPP1R2 LOC105374297 APOD LINC00969 |
nsv1006229 | Chr.3:195350692 - 195747880 on Build GRCh38 | Gain | SDHAP2 MUC20 MUC4 MIR570 ACAP2 PPP1R2 LOC105374297 APOD LINC00969 |
nsv428430 | Chr.3:195478549 - 196102555 on Build GRCh38 | Gain+Loss | SDHAP2 TNK2 MIR570 PPP1R2 APOD SDHAP1 MIR6829 TFRC LOC101929697 LOC105374301 LOC105374299 MUC20 MUC4 LOC105374297 LINC00969 |
esv2763776 | Chr.3:195514028 - 195775248 on Build GRCh38 | Gain+Loss | SDHAP2 MUC20 MUC4 MIR570 PPP1R2 LOC105374297 APOD LINC00969 |
dgv5014n100 | Chr.3:195514016 - 195747880 on Build GRCh38 | Gain | SDHAP2 MUC20 MUC4 MIR570 PPP1R2 LOC105374297 APOD LINC00969 |
esv2759213 | Chr.3:195382058 - 196344722 on Build GRCh38 | Gain+Loss | SDHAP2 TM4SF19-TCTEX1D2 TNK2 TM4SF19 MIR570 ZDHHC19 ACAP2 PPP1R2 APOD SDHAP1 MIR6829 TCTEX1D2 PCYT1A TM4SF19-AS1 TFRC LOC101929697 LOC105374301 LOC105374299 MUC20 MUC4 SLC51A LINC00885 LOC105374297 LINC00969 |
More Information
Set Membership: |
Intragenic Non-exonic DGV Variation |