Assay Details
Target Gene Details
Entrez Gene ID: | 50940 |
Gene Name: | phosphodiesterase 11A |
Gene Aliases: |
PPNAD2 |
Location: |
Chr.2:177623249-178108339 on Build GRCh38 |
Assay Gene Location: | Within Exon 24 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
PDE11A | NM_001077196.1 | 17 | 4990 | NP_001070664.1 |
NM_001077197.1 | 21 | 5520 | NP_001070665.1 | |
NM_016953.3 | 20 | 6489 | NP_058649.3 | |
AK127194.1 | 1 | 268 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv583689 | Chr.2:177603280 - 177645092 on Build GRCh38 | Loss | TTC30A PDE11A |
esv3593466 | Chr.2:177618127 - 177839958 on Build GRCh38 | Gain | TTC30A PDE11A LOC105373764 |
nsv583688 | Chr.2:177562912 - 177675565 on Build GRCh38 | Loss | TTC30A PDE11A LOC105373764 |
More Information
Additional Information:
For this assay, SNP(s) [rs74660778] 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 Exonic DGV Variation |