Assay Details
Target Gene Details
Entrez Gene ID: | 11119 |
Gene Name: | butyrophilin subfamily 3 member A1 |
Gene Aliases: |
BT3.1, BTF5, BTN3.1, CD277 |
Location: |
Chr.6:26402237-26415216 on Build GRCh38 |
Assay Gene Location: | Within Intron 8 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| BTN3A1 | NM_001145008.1 | NP_001138480.1 | ||
| NM_001145009.1 | NP_001138481.1 | |||
| NM_007048.5 | NP_008979.3 | |||
| NM_194441.2 | NP_919423.1 | |||
| XM_005248833.2 | XP_005248890.1 | |||
| XM_005248834.3 | XP_005248891.1 | |||
| XM_006714983.2 | XP_006715046.1 | |||
| AK223474.1 | BAD97194.1 | |||
| AK290193.1 | ||||
| AK291162.1 | ||||
| AK295720.1 | ||||
| AK298652.1 | ||||
| AK299327.1 | ||||
| AK311233.1 | ||||
| BC118586.1 | ||||
| BC121800.1 | ||||
| BG744194.1 | ||||
| CB148209.1 | ||||
| U90552.2 | AAB53430.1 | |||
| Y07827.1 | CAA69164.1 |
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 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 |
|
| esv2731730 | Chr.6:26378223 - 26453505 on Build GRCh38 | Deletion |
|
| esv3608402 | Chr.6:26368480 - 26444267 on Build GRCh38 | Loss |
|
| esv2731728 | Chr.6:26377986 - 26415008 on Build GRCh38 | Deletion |
|
| nsv601184 | Chr.6:26379309 - 26451325 on Build GRCh38 | Gain |
|
| esv3890802 | Chr.6:26369321 - 26442557 on Build GRCh38 | Loss |
|
More Information
Additional Information:
For this assay, SNP(s) [rs72500815] 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: |
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Genomic Map