Assay Details
Target Gene Details
Entrez Gene ID: | 131544 |
Gene Name: | crystallin beta-gamma domain containing 3 |
Gene Aliases: |
DKFZp667G2110, vlAKAP |
Location: |
Chr.3:97821930-97944986 on Build GRCh38 |
Assay Gene Location: | Overlaps - Exon 22 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| CRYBG3 | NM_153605.3 | NP_705833.3 | ||
| XM_005247117.4 | XP_005247174.1 | |||
| AF451988.1 | AAP97687.1 | |||
| AK091199.1 | BAC03608.1 | |||
| AK098569.1 | BAC05338.1 | |||
| AK130907.1 | ||||
| AL831927.1 | CAD38587.1 | |||
| BC036247.1 | AAH36247.1 | |||
| BC050394.1 | AAH50394.1 | |||
| BM974654.1 | ||||
| BX647079.1 | ||||
| BX648353.1 | ||||
| CR749313.1 | CAH18168.1 |
Target Gene Details
Entrez Gene ID: | 84864 |
Gene Name: | MYC induced nuclear antigen |
Gene Aliases: |
MDIG, MINA53, NO52, ROX |
Location: |
Chr.3:97941817-97972451 on Build GRCh38 |
Assay Gene Location: | Within Exon 12 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| MINA | NM_001042533.2 | 10 | 2214 | NP_001035998.1 |
| NM_001261829.1 | 10 | 1744 | NP_001248758.1 | |
| NM_032778.5 | 10 | 2211 | NP_116167.3 | |
| NM_153182.3 | 10 | 1747 | NP_694822.2 | |
| XM_005247838.4 | 10 | 1964 | XP_005247895.1 | |
| XM_011513244.2 | 6 | 1476 | XP_011511546.1 | |
| AB083189.1 | 10 | 1850 | BAC16537.1 | |
| AB083190.1 | 10 | 1847 | BAC16358.1 | |
| AK027299.1 | 10 | 1694 | BAB55024.1 | |
| AY302110.3 | 10 | 1917 | AAP59421.1 | |
| AY390536.1 | 10 | 1899 | AAR27293.1 | |
| AY456380.1 | 10 | 1481 | AAR21572.1 | |
| BC014928.1 | 10 | 1901 | AAH14928.1 | |
| CR627479.1 | 9 | 1500 | CAH10679.1 | |
| DQ453796.1 | 10 | 1711 | ABE28016.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv520553 | Chr.3:95905623 - 98010484 on Build GRCh38 | Gain |
|
| nsv1013060 | Chr.3:96856275 - 98493673 on Build GRCh38 | Gain |
|
| nsv1012322 | Chr.3:97894388 - 97985590 on Build GRCh38 | Gain |
|
More Information
Set Membership: |
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Genomic Map