Assay Details
Target Gene Details
Entrez Gene ID: | 2840 |
Gene Name: | G protein-coupled receptor 17 |
Gene Aliases: |
- |
Location: |
Chr.2:127645864-127652639 on Build GRCh38 |
Assay Gene Location: | Within Exon 4 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| GPR17 | NM_001161415.1 | 4 | 1964 | NP_001154887.1 |
| NM_001161416.1 | 3 | 1899 | NP_001154888.1 | |
| NM_001161417.1 | 2 | 1670 | NP_001154889.1 | |
| NM_005291.2 | 3 | 1735 | NP_005282.1 | |
| XM_017003833.1 | 2 | 2091 | XP_016859322.1 | |
| AK126849.1 | 1 | 2925 | ||
| BC031653.1 | 2 | 1349 | AAH31653.1 | |
| BX538082.1 | CAD98006.1 | |||
| Y12546.1 | 3 | 1427 | CAA73144.1 | |
| Z94154.1 | 2 | 1363 | CAB08107.1 | |
| Z94155.1 | 1 | 1147 | CAB08108.1 |
Target Gene Details
Entrez Gene ID: | 55679 |
Gene Name: | LIM zinc finger domain containing 2 |
Gene Aliases: |
LGMD2W, PINCH-2, PINCH2 |
Location: |
Chr.2:127638421-127681786 on Build GRCh38 |
Assay Gene Location: | Within Intron 8 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| LIMS2 | NM_001136037.2 | NP_001129509.2 | ||
| NM_001161403.1 | NP_001154875.1 | |||
| NM_001161404.1 | NP_001154876.1 | |||
| NM_017980.4 | NP_060450.2 | |||
| XM_005263710.2 | XP_005263767.1 | |||
| XM_006712627.3 | XP_006712690.1 | |||
| XM_011511453.1 | XP_011509755.1 | |||
| AF484961.1 | AAM97589.1 | |||
| AF520987.1 | AAM77350.1 | |||
| AF527764.1 | AAQ09011.1 | |||
| AF527765.1 | AAQ09012.1 | |||
| AF527766.1 | AAQ09013.1 | |||
| AF527767.1 | AAQ09014.1 | |||
| AK000906.1 | BAA91419.1 | |||
| AK022470.1 | BAB14047.1 | |||
| AK055363.1 | ||||
| AK091652.1 | ||||
| AK094954.1 | ||||
| AK095790.1 | ||||
| AK123014.1 | ||||
| AK297645.1 | ||||
| BC065816.1 | AAH65816.1 | |||
| DC356496.1 | ||||
| DR006887.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| dgv4069n100 | Chr.2:127537744 - 127722066 on Build GRCh38 | Gain |
|
| nsv508864 | Chr.2:127585891 - 127684658 on Build GRCh38 | Insertion |
|
| nsv953155 | Chr.2:127617926 - 127665326 on Build GRCh38 | Deletion |
|
| nsv470482 | Chr.2:127593233 - 127707973 on Build GRCh38 | Loss |
|
| nsv583038 | Chr.2:127641265 - 127718910 on Build GRCh38 | Loss |
|
More Information
Set Membership: |
|

Genomic Map