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

Chr.14:104967433 on build GRCh38
Cytoband
14q32.33
Assay ID Hs03889062_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 GPR132 AHNAK2 C14orf79 CDCA4
esv3635634 Chr.14:104965985 - 105147574 on Build GRCh38 Gain JAG2 LOC102723354 GPR132 AHNAK2 C14orf79 CDCA4
nsv1049253 Chr.14:104918622 - 105005518 on Build GRCh38 Gain PLD4 AHNAK2 C14orf79
nsv952276 Chr.14:104922864 - 105021963 on Build GRCh38 Deletion PLD4 AHNAK2 C14orf79 CDCA4
nsv1054574 Chr.14:103210111 - 105365114 on Build GRCh38 Loss LOC102723354 EIF5 LOC105370687 SIVA1 TDRD9 MIR203A NUDT14 INF2 LOC105378183 BAG5 C14orf79 ZBTB42 CDCA4 BRF1 AKT1 KLC1 ASPG MARK3 LINC00638 BTBD6 AHNAK2 LOC105370691 C14orf2 MIR6765 APOPT1 C14orf180 CEP170B PLD4 GPR132 RD3L ZFYVE21 XRCC3 LINC00637 LOC388022 LOC105370708 LOC101929634 TRMT61A JAG2 SNORA28 ADSSL1 CKB TMEM179 LOC107984648 MIR203B KIF26A PACS2 PPP1R13B MIR4710
nsv1052190 Chr.14:104957424 - 105256316 on Build GRCh38 Gain MIR6765 JAG2 LOC102723354 GPR132 NUDT14 BTBD6 AHNAK2 C14orf79 CDCA4 BRF1

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More Information


Additional Information:

For this assay, SNP(s) [rs111431708] 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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