Genomic Map
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Target Gene Details
Entrez Gene ID: | 2649 |
Gene Name: | nuclear receptor subfamily 6 group A member 1 |
Gene Aliases: |
CT150, GCNF, GCNF1, NR61, RTR, hGCNF, hRTR |
Location: |
Chr.9:124517275-124771310 on Build GRCh38 |
Assay Gene Location: | Overlaps - Exon 11 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| NR6A1 | NM_001278546.1 | NP_001265475.1 | ||
| NM_001489.4 | NP_001480.3 | |||
| NM_033334.3 | NP_201591.2 | |||
| XM_005251917.4 | XP_005251974.1 | |||
| XM_005251918.4 | XP_005251975.1 | |||
| AA467752.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv526209 | Chr.9:124470928 - 124531906 on Build GRCh38 | Gain |
 NR6A1
ADGRD2
NR5A1
|
| nsv466559 | Chr.9:124467839 - 124526939 on Build GRCh38 | Loss |
NR6A1
ADGRD2
NR5A1
|
| nsv466558 | Chr.9:124464413 - 124557925 on Build GRCh38 | Loss |
NR6A1
ADGRD2
NR5A1
|
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Additional Information:
For this assay, SNP(s) [rs78761066,rs80250714] 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
|
Gene Ontology Categories:
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