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

Chr.14:104972626 on build GRCh38
Cytoband
14q32.33
Assay ID Hs04440569_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 1
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
AHNAK2 NM_138420.2 NP_612429.2

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

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More Information


Additional Information:

For this assay, SNP(s) [rs73357588] 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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