Assay Details
Target Gene Details
Entrez Gene ID: | 9141 |
Gene Name: | programmed cell death 5 |
Gene Aliases: |
TFAR19 |
Location: |
Chr.19:32581161-32587452 on Build GRCh38 |
Assay Gene Location: | Within Exon 4 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
PDCD5 | NM_004708.3 | NP_004699.1 | ||
XM_005259392.4 | 4 | 1578 | XP_005259449.1 | |
AB209040.1 | 3 | 4950 | BAD92277.1 | |
AF014955.1 | AAD11579.1 | |||
AK124774.1 | 1 | 3169 | ||
BC015519.2 | AAH15519.1 | |||
BM696336.1 | ||||
BT006694.1 | AAP35340.1 | |||
CR456934.1 | CAG33215.1 | |||
DN915905.1 | ||||
DQ208400.1 | ABA60375.1 | |||
N40187.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv519794 | Chr.19:32585709 - 32594595 on Build GRCh38 | Gain |
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More Information
Additional Information:
For this assay, SNP(s) [rs78232320] 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:
