Assay Details
Target Gene Details
Entrez Gene ID: | 576 |
Gene Name: | adhesion G protein-coupled receptor B2 |
Gene Aliases: |
BAI2 |
Location: |
Chr.1:31727105-31764063 on Build GRCh38 |
Assay Gene Location: | Within Exon 30 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
ADGRB2 | NM_001294335.1 | 31 | 4821 | NP_001281264.1 |
NM_001294336.1 | 30 | 4722 | NP_001281265.1 | |
XM_011541848.2 | 30 | 4778 | XP_011540150.1 | |
XM_011541849.2 | 29 | 4613 | XP_011540151.1 | |
XM_011541858.2 | 28 | 3777 | XP_011540160.1 | |
XM_017001899.1 | 30 | 4908 | XP_016857388.1 | |
XM_017001900.1 | 29 | 4877 | XP_016857389.1 | |
XM_017001901.1 | 29 | 4880 | XP_016857390.1 | |
XM_017001902.1 | 29 | 4878 | XP_016857391.1 | |
XM_017001903.1 | 28 | 4812 | XP_016857392.1 | |
XM_017001904.1 | 28 | 4778 | XP_016857393.1 | |
XM_017001905.1 | 28 | 4777 | XP_016857394.1 | |
XM_017001906.1 | 28 | 4779 | XP_016857395.1 | |
XM_017001907.1 | 28 | 4712 | XP_016857396.1 | |
XM_017001908.1 | 28 | 4713 | XP_016857397.1 | |
XM_017001909.1 | 28 | 4714 | XP_016857398.1 | |
XM_017001910.1 | 27 | 4613 | XP_016857399.1 | |
XM_017001911.1 | 27 | 4614 | XP_016857400.1 | |
XM_017001912.1 | 27 | 4546 | XP_016857401.1 | |
AB005298.1 | 31 | 4793 | BAA25362.1 | |
AK123392.1 | 9 | 1911 | ||
AK294361.1 | 10 | 1334 | ||
AK296502.1 | 25 | 3357 | ||
BC009035.1 | 3 | 580 | AAH09035.1 | |
BC136533.1 | 28 | 4390 | ||
BE379230.1 | 3 | 493 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv950385 | Chr.1:31655500 - 31800799 on Build GRCh38 | Deletion | MIR4254 SPOCD1 COL16A1 ADGRB2 |
nsv1007786 | Chr.1:31725560 - 31830924 on Build GRCh38 | Gain | MIR4254 SPOCD1 ADGRB2 |
nsv461028 | Chr.1:31699894 - 31749577 on Build GRCh38 | Loss | COL16A1 ADGRB2 |
esv2758930 | Chr.1:31209533 - 32000730 on Build GRCh38 | Loss | MIR4254 PTP4A2 HCRTR1 SNRNP40 FABP3 NKAIN1 ADGRB2 PEF1 SPOCD1 SERINC2 COL16A1 LINC01225 LINC01226 ZCCHC17 TINAGL1 |
More Information
Set Membership: |
Intragenic Exonic DGV Variation |