Genomic Map
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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 1 - Exon 2 |
| 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 | |||
| AB185926.1 | BAE47454.1 | |||
| AB185927.1 | BAE47455.1 | |||
| AK026345.1 | BAB15456.1 | |||
| BC137503.1 | ||||
| BC137504.1 | ||||
| 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 |
 PLEKHO2
ANKDD1A
PIF1
RBPMS2
MIR1272
|
| dgv31n68 | Chr.15:64706333 - 64929392 on Build GRCh38 | Loss |
PLEKHO2
ANKDD1A
PIF1
RBPMS2
MIR1272
|
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Additional Information:
For this assay, SNP(s) [rs72744802] 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
Non-exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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