Assay Details
Target Gene Details
Entrez Gene ID: | 6095 |
Gene Name: | RAR related orphan receptor A |
Gene Aliases: |
NR1F1, ROR1, ROR2, ROR3, RZR-ALPHA, RZRA |
Location: |
Chr.15:60488284-61229303 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 18 - Exon 19 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
RORA | NM_002943.3 | NP_002934.1 | ||
NM_134260.2 | NP_599022.1 | |||
NM_134261.2 | NP_599023.1 | |||
NM_134262.2 | NP_599024.1 | |||
XM_005254584.4 | XP_005254641.1 | |||
XM_011521874.1 | XP_011520176.1 | |||
XM_011521875.1 | XP_011520177.1 | |||
XM_011521877.2 | XP_011520179.1 | |||
XM_011521878.1 | XP_011520180.1 | |||
XM_011521879.2 | XP_011520181.1 | |||
XM_017022466.1 | XP_016877955.1 | |||
XM_017022467.1 | XP_016877956.1 | |||
AB307694.1 | ||||
BC008831.2 | AAH08831.1 | |||
BC100987.2 | AAI00988.1 | |||
BC100988.1 | AAI00989.1 | |||
BC100989.1 | AAI00990.1 | |||
BC100990.2 | AAI00991.1 | |||
HQ692818.1 | ||||
HQ709174.1 | ||||
L14611.1 | AAA02963.1 | |||
U04897.1 | AAA62658.1 | |||
U04898.1 | AAA62659.1 | |||
U04899.1 | AAA62660.1 |
Target Gene Details
Entrez Gene ID: | 101928784 |
Gene Name: | RORA antisense RNA 1 |
Gene Aliases: |
- |
Location: |
Chr.15:60479178-60630639 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
RORA-AS1 | NR_120339.1 | |||
NR_120340.1 | ||||
NR_120341.1 | ||||
NR_120342.1 | ||||
AW663525.1 | ||||
BI668481.1 | ||||
BX115309.1 | ||||
DA507239.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv569609 | Chr.15:60417705 - 60502450 on Build GRCh38 | Loss | ICE2 RORA-AS1 RORA |
nsv527607 | Chr.15:60454406 - 60507710 on Build GRCh38 | Loss | ICE2 RORA-AS1 RORA |
nsv525689 | Chr.15:60448642 - 60531218 on Build GRCh38 | Gain | ICE2 RORA-AS1 RORA |
More Information
Set Membership: |
Intragenic Intronic Non-exonic DGV Variation |