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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 C14orf79 AHNAK2
nsv566141 Chr.14:104938047 - 105089059 on Build GRCh38 Gain C14orf79 AHNAK2 CDCA4 GPR132
esv3635634 Chr.14:104965985 - 105147574 on Build GRCh38 Gain C14orf79 AHNAK2 LOC102723354 CDCA4 GPR132 JAG2
nsv952276 Chr.14:104922864 - 105021963 on Build GRCh38 Deletion C14orf79 AHNAK2 CDCA4 PLD4
nsv1049253 Chr.14:104918622 - 105005518 on Build GRCh38 Gain C14orf79 AHNAK2 PLD4
nsv1054574 Chr.14:103210111 - 105365114 on Build GRCh38 Loss RD3L BAG5 MIR4710 MIR6765 APOPT1 MIR203B SNORA28 PPP1R13B EIF5 C14orf2 SIVA1 PACS2 LOC101929634 JAG2 AKT1 ASPG XRCC3 LOC105378183 AHNAK2 LOC102723354 KLC1 TDRD9 C14orf180 LINC00637 MARK3 C14orf79 CEP170B CKB BTBD6 LOC105370687 TMEM179 ZFYVE21 LINC00638 GPR132 LOC388022 NUDT14 KIF26A TRMT61A ZBTB42 ADSSL1 MIR203A BRF1 LOC105370691 CDCA4 INF2 LOC105370708 PLD4 LOC107984648
nsv1052190 Chr.14:104957424 - 105256316 on Build GRCh38 Gain MIR6765 C14orf79 BTBD6 BRF1 AHNAK2 LOC102723354 CDCA4 GPR132 JAG2 NUDT14
nsv566150 Chr.14:104969312 - 105223755 on Build GRCh38 Loss MIR6765 C14orf79 BRF1 AHNAK2 LOC102723354 CDCA4 GPR132 JAG2 NUDT14

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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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