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Gene Symbol
PRPF4B
Assay Reference Genome
Location

Chr.6:4020766 on build GRCh38
Cytoband
6p25.2
Assay ID Hs06804936_cn
Size
Availability Made To Order
Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 8899

Gene Name:

 pre-mRNA processing factor 4B

Gene Aliases:

 PR4H, PRP4, PRP4H, PRP4K, dJ1013A10.1

Location:

 Chr.6:4019402-4064983 on Build GRCh38

Assay Gene Location:

 Within Exon 1
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
PRPF4B XM_011514970.2 1 1365 XP_011513272.1
XM_017011410.1 1 1365 XP_016866899.1
XM_017011411.1 1 1365 XP_016866900.1
XM_017011412.1 1 1365 XP_016866901.1
XM_017011413.1 1 1365 XP_016866902.1
XM_017011414.1 1 1365 XP_016866903.1
XM_017011415.1 1 1365 XP_016866904.1
XM_017011416.1 1 1365 XP_016866905.1
XM_017011417.1 1 1365 XP_016866906.1
XM_017011418.1 1 1365 XP_016866907.1
XM_017011419.1 1 1365 XP_016866908.1
XM_017011420.1 1 1365 XP_016866909.1
XM_017011421.1 1 1365 XP_016866910.1
XM_017011422.1 1 1365 XP_016866911.1
XM_017011423.1 1 1365 XP_016866912.1
XM_017011424.1 1 1365 XP_016866913.1
XM_017011425.1 1 1365 XP_016866914.1
XM_017011426.1 1 1365 XP_016866915.1
XM_017011427.1 1 1365 XP_016866916.1
XM_017011428.1 1 1365 XP_016866917.1
XM_017011429.1 1 1365 XP_016866918.1
XM_017011430.1 1 1365 XP_016866919.1
XM_017011431.1 1 1365 XP_016866920.1
XM_017011432.1 1 1365 XP_016866921.1
XM_017011433.1 1 1365 XP_016866922.1
XM_017011434.1 1 1365 XP_016866923.1
XM_017011435.1 1 1365 XP_016866924.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv1140598 Chr.6:4020778 - 4020828 on Build GRCh38 Deletion PRPF4B
nsv1074366 Chr.6:4020777 - 4020828 on Build GRCh38 Deletion PRPF4B
esv2731499 Chr.6:4020698 - 4020988 on Build GRCh38 Deletion PRPF4B
esv2370815 Chr.6:4020581 - 4021022 on Build GRCh38 Deletion PRPF4B
esv2493637 Chr.6:4020781 - 4020830 on Build GRCh38 Deletion PRPF4B
esv1658451 Chr.6:4020780 - 4020830 on Build GRCh38 Deletion PRPF4B
esv2731500 Chr.6:4020812 - 4020935 on Build GRCh38 Deletion PRPF4B

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More Information


Additional Information:

For this assay, SNP(s) [rs567961417] 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 Exonic DGV Variation

Gene Ontology Categories:

Function(s) Process(es)


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