Assay Details
Target Gene Details
Entrez Gene ID: | 81575 |
Gene Name: | apolipoprotein L domain containing 1 |
Gene Aliases: |
VERGE |
Location: |
Chr.12:12725917-12791466 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
APOLD1 | NM_001130415.1 | NP_001123887.1 | ||
BC042478.1 | AAH42478.1 | |||
DC413327.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv2745567 | Chr.12:12246086 - 13092998 on Build GRCh38 | Deletion | RPL13AP20 LOC100506314 DUSP16 CDKN1B MIR614 GPRC5D CREBL2 FAM234B HTR7P1 MANSC1 DDX47 BORCS5 LOC105369662 LRP6 LOH12CR2 MIR613 GSG1 APOLD1 GPRC5A GPR19 HEBP1 |
nsv53843 | Chr.12:12750387 - 12754202 on Build GRCh38 | Deletion | APOLD1 |
nsv1046355 | Chr.12:11501836 - 12890185 on Build GRCh38 | Loss | RPL13AP20 DUSP16 CDKN1B CREBL2 ETV6 MANSC1 DDX47 LOC100506248 BORCS5 LOC105369662 LRP6 LOH12CR2 BCL2L14 MIR613 APOLD1 GPR19 LINC01252 MIR1244-4 |
More Information
Additional Information:
For this assay, SNP(s) [rs78448659] 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 |