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See other ZNF496 CNV Assays ›
Gene Symbol
ZNF496
Assay Reference Genome
Location

Chr.1:247316881 on build GRCh38
Cytoband
1q44
Assay ID Hs03332632_cn
Size
Availability Made To Order
Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 84838

Gene Name:

 zinc finger protein 496

Gene Aliases:

 NIZP1, ZFP496, ZKSCAN17, ZSCAN49

Location:

 Chr.1:247297413-247333376 on Build GRCh38

Assay Gene Location:

 Within Intron 7
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
ZNF496 NM_032752.1 NP_116141.1
XM_005273328.3 XP_005273385.1
XM_005273330.3 XP_005273387.1
XM_006711838.2 XP_006711901.1
XM_011544310.1 XP_011542612.1
XM_011544312.1 XP_011542614.1
XM_011544314.2 XP_011542616.1
XM_011544315.2 XP_011542617.1
XM_011544316.1 XP_011542618.1
XM_017002586.1 XP_016858075.1
XM_017002587.1 XP_016858076.1
XM_017002588.1 XP_016858077.1
XM_017002589.1 XP_016858078.1
XM_017002590.1 XP_016858079.1
XM_017002591.1 XP_016858080.1
XM_017002592.1 XP_016858081.1
XM_017002593.1 XP_016858082.1
AK098030.1
AK310669.1
BC007263.1 AAH07263.1
BC025794.1 AAH25794.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv833137 Chr.1:247274015 - 247444126 on Build GRCh38 Gain LOC107985115 NLRP3 ZNF496
esv33129 Chr.1:246911128 - 248165533 on Build GRCh38 Gain+Loss OR2M1P ZNF669 ZNF670 OR2W3 AHCTF1 ZNF695 OR1C1 ZNF124 LOC107985115 OR2L3 OR2T8 OR2L1P OR2W5 OR9H1P OR2L5 TRIM58 VN1R5 OR11L1 OR2L2 MIR3916 OR6F1 OR2G3 OR14A16 NLRP3 OR2L8 ZNF670-ZNF695 OR13G1 OR2G2 ZNF496 C1orf229 GCSAML-AS1 OR2M5 OR2C3 OR2L13 OR2AK2 GCSAML OR2B11
esv3589514 Chr.1:247297392 - 247354590 on Build GRCh38 Gain LOC107985115 ZNF496
nsv509790 Chr.1:247311000 - 247445876 on Build GRCh38 Insertion LOC107985115 NLRP3 ZNF496

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More Information


Additional Information:

For this assay, SNP(s) [rs79543803] 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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