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See other AHNAK2 CNV Assays ›
Gene Symbol
AHNAK2
Assay Reference Genome
Location

Chr.14:104970079 on build GRCh38
Cytoband
14q32.33
Assay ID Hs03880835_cn
Size
Availability Made To Order
Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 113146

Gene Name:

 AHNAK nucleoprotein 2

Gene Aliases:

 C14orf78

Location:

 Chr.14:104937253-104978357 on Build GRCh38

Assay Gene Location:

 Within Intron 2
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
AHNAK2 NM_138420.2 NP_612429.2
XM_005267299.1 XP_005267356.1
AK094143.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv1438 Chr.14:104946391 - 104991244 on Build GRCh38 Deletion AHNAK2 C14orf79
nsv566141 Chr.14:104938047 - 105089059 on Build GRCh38 Gain AHNAK2 CDCA4 C14orf79 GPR132
esv3635634 Chr.14:104965985 - 105147574 on Build GRCh38 Gain AHNAK2 CDCA4 C14orf79 GPR132 JAG2 LOC102723354
nsv1049253 Chr.14:104918622 - 105005518 on Build GRCh38 Gain AHNAK2 C14orf79 PLD4
nsv952276 Chr.14:104922864 - 105021963 on Build GRCh38 Deletion AHNAK2 CDCA4 C14orf79 PLD4
nsv1054574 Chr.14:103210111 - 105365114 on Build GRCh38 Loss PACS2 KIF26A BAG5 CDCA4 LOC105370687 BTBD6 MIR203B GPR132 LINC00637 RD3L EIF5 MARK3 MIR6765 TDRD9 PPP1R13B MIR4710 PLD4 CEP170B LOC105370691 AHNAK2 APOPT1 TRMT61A LOC105378183 XRCC3 AKT1 MIR203A C14orf180 SIVA1 ADSSL1 ZFYVE21 KLC1 LINC00638 ZBTB42 ASPG C14orf79 JAG2 LOC107984648 CKB LOC102723354 BRF1 SNORA28 NUDT14 LOC101929634 TMEM179 C14orf2 INF2 LOC105370708 LOC388022
nsv1052190 Chr.14:104957424 - 105256316 on Build GRCh38 Gain BRF1 AHNAK2 NUDT14 CDCA4 BTBD6 C14orf79 GPR132 JAG2 MIR6765 LOC102723354
nsv456458 Chr.14:104969312 - 105223755 on Build GRCh38 Loss BRF1 AHNAK2 NUDT14 CDCA4 C14orf79 GPR132 JAG2 MIR6765 LOC102723354

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More Information


Additional Information:

For this assay, SNP(s) [rs151130395] 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

Gene Ontology Categories:

Function(s) Process(es)


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