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See other APBA2 CNV Assays ›
Gene Symbol
APBA2
Assay Reference Genome
Location

Chr.15:28937083 on build GRCh38
Cytoband
15q13.1
Assay ID Hs05389851_cn
Size
Availability Made To Order
Catalog # 4400291
Price
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Assay Details

Target Gene Details

Entrez Gene ID:

 321

Gene Name:

 amyloid beta precursor protein binding family A member 2

Gene Aliases:

 D15S1518E, HsT16821, LIN-10, MGC:14091, MINT2, X11-BETA, X11L

Location:

 Chr.15:28885479-29118315 on Build GRCh38

Assay Gene Location:

 Within Intron 6
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
APBA2 NM_001130414.1 NP_001123886.1
NM_005503.3 NP_005494.2
XM_011521488.2 XP_011519790.1
XM_011521489.2 XP_011519791.1
XM_011521490.2 XP_011519792.1
XM_011521493.2 XP_011519795.1
XM_011521494.2 XP_011519796.1
XM_017022101.1 XP_016877590.1
XM_017022102.1 XP_016877591.1
XM_017022103.1 XP_016877592.1
XM_017022104.1 XP_016877593.1
XM_017022105.1 XP_016877594.1
XM_017022106.1 XP_016877595.1
XM_017022107.1 XP_016877596.1
XM_017022108.1 XP_016877597.1
XM_017022109.1 XP_016877598.1
XM_017022110.1 XP_016877599.1
XM_017022111.1 XP_016877600.1
XM_017022113.1 XP_016877602.1
XM_017022114.1 XP_016877603.1
XM_017022115.1 XP_016877604.1
XM_017022117.1 XP_016877606.1
AF047348.1 AAC39767.1
AK310413.1
BC082986.1 AAH82986.1
BX332225.2

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv1040778 Chr.15:28689598 - 30515727 on Build GRCh38 Loss GOLGA8M CHRFAM7A ULK4P3 WHAMMP2 LOC100130111 APBA2 TJP1 LOC100289656 GOLGA8J GOLGA8T LOC101060569 GOLGA8R LOC105370746 GOLGA6L7P DKFZP434L187 LOC107984752 NSMCE3 PDCD6IPP2 LOC105370751 FAM189A1
nsv527255 Chr.15:28754022 - 30074044 on Build GRCh38 Gain GOLGA6L7P WHAMMP2 LOC107984752 LOC100130111 APBA2 TJP1 LOC100289656 NSMCE3 PDCD6IPP2 FAM189A1
esv2751526 Chr.15:28724519 - 30687025 on Build GRCh38 Loss CHRFAM7A ARHGAP11B WHAMMP2 LOC100289656 GOLGA8R GOLGA6L7P DKFZP434L187 LOC107984752 LOC100288637 ULK4P2 NSMCE3 PDCD6IPP2 LOC105370751 LOC100996413 GOLGA8H ULK4P3 LOC100130111 APBA2 TJP1 GOLGA8J GOLGA8T LOC101060569 LOC105370746 LOC101927579 FAM189A1
nsv1039798 Chr.15:28724126 - 30158154 on Build GRCh38 Gain ULK4P3 WHAMMP2 LOC100130111 APBA2 TJP1 LOC100289656 GOLGA8J GOLGA8T GOLGA6L7P LOC107984752 NSMCE3 PDCD6IPP2 FAM189A1
nsv516384 Chr.15:28920744 - 28996217 on Build GRCh38 Loss APBA2
nsv1038806 Chr.15:28933682 - 28965543 on Build GRCh38 Gain APBA2
nsv568662 Chr.15:27726493 - 29056123 on Build GRCh38 Gain GOLGA8M MIR4509-2 GOLGA8F HERC2P9 OCA2 WHAMMP2 APBA2 LOC100289656 HERC2 GOLGA8G LOC100132202 MIR4509-3 GOLGA6L7P LOC107984752 LOC101929047 PDCD6IPP2 LOC645202 HERC2P11

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More Information


Additional Information:

For this assay, SNP(s) [rs67366736] 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

Panther Classification:

Gene Ontology Categories:

Function(s) Process(es)


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