Assay Details
Target Gene Details
Entrez Gene ID: | 23646 |
Gene Name: | phospholipase D family member 3 |
Gene Aliases: |
AD19, HU-K4, HUK4 |
Location: |
Chr.19:40348395-40378490 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
PLD3 | NM_001031696.3 | NP_001026866.1 | ||
NM_012268.3 | NP_036400.2 | |||
XM_005258704.1 | XP_005258761.1 | |||
XM_005258707.4 | XP_005258764.1 | |||
XM_005258708.3 | XP_005258765.1 | |||
XM_005258709.4 | XP_005258766.1 | |||
XM_005258710.4 | XP_005258767.1 | |||
XM_006723122.1 | XP_006723185.1 | |||
XM_011526692.1 | XP_011524994.1 | |||
XM_011526693.1 | XP_011524995.1 | |||
XM_017026546.1 | XP_016882035.1 | |||
XM_017026547.1 | XP_016882036.1 | |||
XM_017026548.1 | XP_016882037.1 | |||
XM_017026549.1 | XP_016882038.1 | |||
AK293690.1 | ||||
BC036327.1 | AAH36327.1 | |||
BC096820.1 | AAH96820.1 | |||
CX785201.1 | ||||
DA370667.1 | ||||
DB057420.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv3644346 | Chr.19:40355360 - 40358314 on Build GRCh38 | Loss |
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nsv833831 | Chr.19:40290833 - 40454958 on Build GRCh38 | Loss |
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esv2665673 | Chr.19:40355389 - 40358343 on Build GRCh38 | Deletion |
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![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)
More Information
Additional Information:
For this assay, SNP(s) [rs73046335] 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: |
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Panther Classification:
Gene Ontology Categories:
![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)