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: | Within Exon 22 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
CRYBG3 | NM_153605.3 | 22 | 9785 | NP_705833.3 |
XM_005247117.4 | 21 | 9488 | XP_005247174.1 | |
AF451988.1 | 10 | 1902 | AAP97687.1 | |
AK091199.1 | 14 | 2256 | BAC03608.1 | |
AK098569.1 | BAC05338.1 | |||
AK130907.1 | 2 | 797 | ||
AL831927.1 | 10 | 1808 | CAD38587.1 | |
BC036247.1 | 5 | 1328 | AAH36247.1 | |
BC050394.1 | 7 | 1568 | AAH50394.1 | |
BX647079.1 | 14 | 2273 | ||
BX648353.1 | 19 | 3835 | ||
CR749313.1 | 19 | 2910 | 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 | 3140 | NP_001035998.1 |
NM_001261829.1 | 10 | 2670 | NP_001248758.1 | |
NM_032778.5 | 10 | 3137 | NP_116167.3 | |
NM_153182.3 | 10 | 2673 | NP_694822.2 | |
XM_005247838.4 | 10 | 2890 | XP_005247895.1 |
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 | GABRR3 EPHA6 ARL6 MIR8060 MINA CRYBG3 |
nsv1013060 | Chr.3:96856275 - 98493673 on Build GRCh38 | Gain | OR5H1 GABRR3 OR5H2 OR5H15 ARL6 OR5K1 OR5AC2 OR5K3 MINA OR5H14 OR5H6 EPHA6 OR5K4 CRYBG3 |
nsv1012322 | Chr.3:97894388 - 97985590 on Build GRCh38 | Gain | MINA CRYBG3 |
More Information
Additional Information:
For this assay, SNP(s) [rs78729642] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Set Membership: |
Intragenic Exonic DGV Variation |