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Gene Symbol
WFDC3
Assay Reference Genome
Location

Chr.20:45748308 on build GRCh38
Cytoband
20q13.12
Assay ID Hs04041596_cn
Size
Availability Made To Order
Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 140686

Gene Name:

 WAP four-disulfide core domain 3

Gene Aliases:

 WAP14, dJ447F3.3

Location:

 Chr.20:45708860-45791908 on Build GRCh38

Assay Gene Location:

 Within Intron 9
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
WFDC3 XM_017027668.1 XP_016883157.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
esv2751916 Chr.20:45722292 - 45771812 on Build GRCh38 Loss WFDC3 SPINT4
dgv512n27 Chr.20:45726581 - 45749938 on Build GRCh38 Loss WFDC3
dgv7592n54 Chr.20:45722456 - 45749938 on Build GRCh38 Loss WFDC3 SPINT4
esv33602 Chr.20:45722083 - 45750234 on Build GRCh38 Loss WFDC3 SPINT4
dgv7590n54 Chr.20:45709047 - 45749938 on Build GRCh38 Loss WFDC3 SPINT4
esv2670845 Chr.20:45744160 - 45758866 on Build GRCh38 Deletion WFDC3
dgv4320n100 Chr.20:45713700 - 45758128 on Build GRCh38 Loss WFDC3 SPINT4
esv2678145 Chr.20:45720211 - 45750898 on Build GRCh38 Deletion WFDC3 SPINT4
nsv586131 Chr.20:45727555 - 45778454 on Build GRCh38 Loss WFDC3
esv3645940 Chr.20:45744194 - 45758836 on Build GRCh38 Loss WFDC3
nsv1058157 Chr.20:45729036 - 45749572 on Build GRCh38 Loss WFDC3
esv3557119 Chr.20:45720144 - 45750978 on Build GRCh38 Deletion WFDC3 SPINT4
esv2763671 Chr.20:45719923 - 45752208 on Build GRCh38 Loss WFDC3 SPINT4
esv3645939 Chr.20:45719986 - 45751040 on Build GRCh38 Loss WFDC3 SPINT4
dgv4321n100 Chr.20:45719911 - 45754523 on Build GRCh38 Loss WFDC3 SPINT4
dgv1247e212 Chr.20:45708247 - 45752976 on Build GRCh38 Loss WFDC10B WFDC13 WFDC3 SPINT4
esv2751915 Chr.20:45708077 - 45749572 on Build GRCh38 Loss WFDC10B WFDC13 WFDC3 SPINT4

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More Information


Additional Information:

For this assay, SNP(s) [rs78256458] 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:

Molecular Function -

protease inhibitor

Gene Ontology Categories:

Function(s) Process(es)


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