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Gene Symbol
BTN3A3
Assay Reference Genome
Location

Chr.6:26452896 on build GRCh38
Cytoband
6p22.2
Assay ID Hs03025684_cn
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Catalog # 4400291
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Assay Details

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 11
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
BTN3A3 NM_001242803.1 6 1828 NP_001229732.1
NM_006994.4 11 2483 NP_008925.1
NM_197974.2 10 2391 NP_932078.2
AB209581.1 7 4011 BAD92818.1
AK223301.1 11 2402 BAD97021.1
BC015815.2 11 2420 AAH15815.1
U90548.1 11 2411 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 HIST1H2AD BTN3A2 HIST1H4C BTN1A1 HIST1H3D HFE HIST1H2AC HIST1H4E HIST1H2BE HIST1H1C HIST1H3A HIST1H3B BTN3A3 SLC17A2 HIST1H1E BTN2A2 HIST1H3C HIST1H2BB HIST1H1D BTN2A3P HIST1H4A HIST1H4F HCG11 HIST1H2AB HIST1H3G SLC17A3 HIST1H4D TRIM38 HIST1H4H HIST1H4G HIST1H4B HIST1H3E HIST1H2BF HIST1H1T HIST1H2BH HIST1H1A BTN2A1 HIST1H2BG HIST1H3F HIST1H2BI HIST1H2BD HIST1H2AE LOC285819 BTN3A1 HIST1H2BC
esv3576106 Chr.6:26428086 - 26463788 on Build GRCh38 Gain BTN3A2 BTN2A1 BTN2A3P BTN3A3
esv2731730 Chr.6:26378223 - 26453505 on Build GRCh38 Deletion BTN3A2 BTN2A2 BTN2A3P BTN3A3 BTN3A1
nsv969359 Chr.6:26443433 - 26453013 on Build GRCh38 Duplication BTN3A2 BTN3A3
nsv528172 Chr.6:26430753 - 26463432 on Build GRCh38 Loss BTN3A2 BTN2A1 BTN3A3
nsv1017824 Chr.6:26425182 - 26465156 on Build GRCh38 Gain+Loss BTN3A2 BTN2A1 BTN2A3P BTN3A3
esv2763996 Chr.6:26423673 - 26465156 on Build GRCh38 Gain BTN3A2 BTN2A1 BTN2A3P BTN3A3

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More Information


Additional Information:

For this assay, SNP(s) [rs80165853] 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

Panther Classification:

Gene Ontology Categories:

Function(s)


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