Assay Details
Target Gene Details
Entrez Gene ID: | 5738 |
Gene Name: | prostaglandin F2 receptor inhibitor |
Gene Aliases: |
CD315, CD9P-1, EWI-F, FPRP, SMAP-6 |
Location: |
Chr.1:116909923-116990358 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
PTGFRN | NM_020440.3 | NP_065173.2 | ||
AB037857.1 | ||||
AK074637.1 | BAC11104.1 | |||
BC098142.1 | AAH98142.1 | |||
BC114520.1 | AAI14521.1 | |||
BC139718.1 | ||||
BC152454.1 | ||||
DA572787.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv831159 | Chr.1:116844705 - 117040990 on Build GRCh38 | Loss | CD101 LOC101929099 PTGFRN |
nsv547586 | Chr.1:116897441 - 116930081 on Build GRCh38 | Loss | PTGFRN |
nsv2566 | Chr.1:116871424 - 116916532 on Build GRCh38 | Deletion | PTGFRN |
More Information
Additional Information:
For this assay, SNP(s) [rs73012706] 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 Intronic Non-exonic DGV Variation |