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: | Within Intron 8 |
| 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 | |||
| AF004291.1 | AAC52054.1 | |||
| BC030600.1 | AAH30600.1 | |||
| HQ692858.1 | ||||
| HQ709185.1 | ||||
| S83309.1 | AAB50876.1 | |||
| U80802.1 | AAB96828.1 |
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 |
 ADGRD2
NR5A1
NR6A1
|
| nsv6712 | Chr.9:124522641 - 124546161 on Build GRCh38 | Deletion |
NR6A1
|
| nsv466558 | Chr.9:124464413 - 124557925 on Build GRCh38 | Loss |
ADGRD2
NR5A1
NR6A1
|
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Set Membership: |
Intragenic
Intronic
Non-exonic
DGV Variation
|
Gene Ontology Categories:
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