Assay Details
Target Gene Details
Entrez Gene ID: | 3164 |
Gene Name: | nuclear receptor subfamily 4 group A member 1 |
Gene Aliases: |
GFRP1, HMR, N10, NAK-1, NGFIB, NP10, NUR77, TR3 |
Location: |
Chr.12:52022832-52059507 on Build GRCh38 |
Assay Gene Location: | Within Exon 6 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
NR4A1 | NM_001202233.1 | NP_001189162.1 | ||
NM_001202234.1 | NP_001189163.1 | |||
XM_005268822.3 | XP_005268879.1 | |||
XM_005268824.3 | XP_005268881.1 | |||
XM_006719363.1 | XP_006719426.1 | |||
XM_006719364.3 | XP_006719427.1 | |||
XM_017019248.1 | 4 | 3903 | XP_016874737.1 | |
XM_017019249.1 | 4 | 3795 | XP_016874738.1 | |
AK131566.1 | BAD18699.1 | |||
AK297526.1 | ||||
AL702926.1 | ||||
D85245.1 | BAA12746.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv469378 | Chr.12:52009326 - 52047766 on Build GRCh38 | Loss | GRASP NR4A1 |
More Information
Additional Information:
For this assay, SNP(s) [rs115818747] 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 Exonic DGV Variation |