Assay Details
Target Gene Details
Entrez Gene ID: | 11118 |
Gene Name: | butyrophilin subfamily 3 member A2 |
Gene Aliases: |
BT3.2, BTF4, BTN3.2, CD277 |
Location: |
Chr.6:26365159-26451697 on Build GRCh38 |
Assay Gene Location: | Within Intron 11 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| BTN3A2 | XM_011514268.2 | XP_011512570.1 |
Target Gene Details
Entrez Gene ID: | 10384 |
Gene Name: | butyrophilin subfamily 3 member A3 |
Gene Aliases: |
BTF3, BTN3.3 |
Location: |
Chr.6:26440472-26453415 on Build GRCh38 |
Assay Gene Location: | Within Exon 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| BTN3A3 | NM_001242803.1 | 1 | 93 | NP_001229732.1 |
| NM_006994.4 | 1 | 93 | NP_008925.1 | |
| NM_197974.2 | 1 | 93 | NP_932078.2 | |
| AB209581.1 | BAD92818.1 | |||
| AK223279.1 | BAD96999.1 | |||
| AK223301.1 | BAD97021.1 | |||
| AK291722.1 | 1 | 77 | ||
| AK301553.1 | 1 | 77 | ||
| BC015815.2 | AAH15815.1 | |||
| BX341863.2 | ||||
| DA445999.1 | 1 | 93 | ||
| DC410234.1 | 1 | 93 | ||
| U90548.1 | AAB53426.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv1023453 | Chr.6:25853602 - 26528022 on Build GRCh38 | Gain |
|
| esv3576106 | Chr.6:26428086 - 26463788 on Build GRCh38 | Gain |
|
| esv2731730 | Chr.6:26378223 - 26453505 on Build GRCh38 | Deletion |
|
| esv3608402 | Chr.6:26368480 - 26444267 on Build GRCh38 | Loss |
|
| nsv528172 | Chr.6:26430753 - 26463432 on Build GRCh38 | Loss |
|
| nsv1017824 | Chr.6:26425182 - 26465156 on Build GRCh38 | Gain+Loss |
|
| nsv601184 | Chr.6:26379309 - 26451325 on Build GRCh38 | Gain |
|
| esv3890802 | Chr.6:26369321 - 26442557 on Build GRCh38 | Loss |
|
| esv2763996 | Chr.6:26423673 - 26465156 on Build GRCh38 | Gain |
|
More Information
Additional Information:
For this assay, SNP(s) [rs114195506] 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: |
|

Genomic Map