Assay Details
Target Gene Details
Entrez Gene ID: | 10886 |
Gene Name: | neuropeptide FF receptor 2 |
Gene Aliases: |
GPR74, HLWAR77, NPFF2, NPGPR |
Location: |
Chr.4:72031804-72148201 on Build GRCh38 |
Assay Gene Location: | Within Intron 3 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
NPFFR2 | NM_001144756.1 | NP_001138228.1 | ||
NM_004885.2 | NP_004876.2 | |||
NM_053036.2 | NP_444264.1 | |||
XM_011531554.2 | XP_011529856.1 | |||
AF119815.1 | AAD22047.1 | |||
AF236083.1 | AAK58513.1 | |||
AF257210.1 | AAF87078.1 | |||
AJ311393.1 | CAC85427.1 | |||
AK290937.1 | ||||
AK308069.1 | ||||
BC101636.1 | ||||
BC113713.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv508287 | Chr.4:72066492 - 72086216 on Build GRCh38 | Deletion | NPFFR2 |
More Information
Additional Information:
For this assay, SNP(s) [rs72856103] 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 |