Assay Details
Target Gene Details
Entrez Gene ID: | 128954 |
Gene Name: | GRB2 associated binding protein family member 4 |
Gene Aliases: |
- |
Location: |
Chr.22:16961936-17008281 on Build GRCh38 |
Assay Gene Location: | Within Intron 4 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
GAB4 | NM_001037814.1 | NP_001032903.1 | ||
XM_011546114.2 | XP_011544416.1 | |||
XM_011546115.1 | XP_011544417.1 | |||
XM_011546116.2 | XP_011544418.1 | |||
XM_011546117.1 | XP_011544419.1 | |||
XM_017028575.1 | XP_016884064.1 | |||
XM_017028576.1 | XP_016884065.1 | |||
AB076978.1 | BAD06454.1 | |||
AK057252.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv2763696 | Chr.22:16384236 - 16983056 on Build GRCh38 | Gain | TPTEP1 ACTR3BP6 GAB4 HSFY1P1 LOC101929350 CCT8L2 ANKRD62P1-PARP4P3 XKR3 |
esv3647204 | Chr.22:16939332 - 17123705 on Build GRCh38 | Gain | CECR6 GAB4 LOC100996342 CECR7 IL17RA |
dgv4460n100 | Chr.22:16384224 - 17135620 on Build GRCh38 | Gain | TPTEP1 ACTR3BP6 CECR6 GAB4 HSFY1P1 LOC100996342 LOC101929350 CCT8L2 CECR7 ANKRD62P1-PARP4P3 IL17RA XKR3 |
nsv588077 | Chr.22:16674094 - 16972076 on Build GRCh38 | Gain | GAB4 HSFY1P1 LOC101929350 ANKRD62P1-PARP4P3 XKR3 |
esv1004225 | Chr.22:16965391 - 16973576 on Build GRCh38 | Deletion | GAB4 |
dgv4463n100 | Chr.22:16749141 - 17081023 on Build GRCh38 | Gain | GAB4 HSFY1P1 CECR7 XKR3 |
nsv527637 | Chr.22:16437596 - 16981295 on Build GRCh38 | Gain | TPTEP1 ACTR3BP6 GAB4 HSFY1P1 LOC101929350 CCT8L2 ANKRD62P1-PARP4P3 XKR3 |
esv3575406 | Chr.22:16408174 - 16982154 on Build GRCh38 | Gain | TPTEP1 ACTR3BP6 GAB4 HSFY1P1 LOC101929350 CCT8L2 ANKRD62P1-PARP4P3 XKR3 |
nsv1064641 | Chr.22:16757380 - 17233805 on Build GRCh38 | Gain | CECR1 CECR6 GAB4 HSFY1P1 LOC100996342 CECR5-AS1 CECR7 IL17RA CECR5 XKR3 |
More Information
Additional Information:
For this assay, SNP(s) [rs73145687] 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 Intronic Non-exonic DGV Variation |