Assay Details
Target Gene Details
Entrez Gene ID: | 80119 |
Gene Name: | PIF1 5'-to-3' DNA helicase |
Gene Aliases: |
C15orf20, PIF |
Location: |
Chr.15:64815630-64827173 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 9 - Exon 9 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
PIF1 | NM_001286496.1 | NP_001273425.1 | ||
NM_001286497.1 | NP_001273426.1 | |||
NM_001286499.1 | NP_001273428.1 | |||
NM_025049.3 | NP_079325.2 | |||
XM_011522083.2 | XP_011520385.1 | |||
XM_011522084.2 | XP_011520386.1 | |||
AB185926.1 | BAE47454.1 | |||
AB185927.1 | BAE47455.1 | |||
AF108138.1 | AAD44047.1 | |||
AY498716.1 | AAS77398.1 | |||
BC137503.1 | ||||
BC137504.1 | ||||
DQ437529.1 | ABD92708.1 | |||
EU084033.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv569703 | Chr.15:64756110 - 64930560 on Build GRCh38 | Loss |
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dgv31n68 | Chr.15:64706333 - 64929392 on Build GRCh38 | Loss |
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esv3636745 | Chr.15:64815095 - 64823057 on Build GRCh38 | Loss |
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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) [rs74778945] 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)