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Gene Symbol
INPP4B
Assay Reference Genome
Location

Chr.4:142047087 on build GRCh38
Cytoband
4q31.21
Assay ID Hs04795646_cn
Size
Availability Made To Order
Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 8821

Gene Name:

 inositol polyphosphate-4-phosphatase type II B

Gene Aliases:

 -

Location:

 Chr.4:142023160-142846535 on Build GRCh38

Assay Gene Location:

 Within Intron 30
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
INPP4B NM_001101669.1 NP_001095139.1
NM_003866.2 NP_003857.2
XM_005263323.3 XP_005263380.1
XM_005263325.3 XP_005263382.1
XM_011532391.2 XP_011530693.1
XM_011532392.2 XP_011530694.1
XM_017008794.1 XP_016864283.1
XM_017008795.1 XP_016864284.1
XM_017008796.1 XP_016864285.1
XM_017008797.1 XP_016864286.1
XM_017008798.1 XP_016864287.1
BC017924.2 AAH17924.1
BC110918.1 AAI10919.1
BC133005.1
BX649090.1
U96922.1 AAB72153.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv830097 Chr.4:142028552 - 142215219 on Build GRCh38 Gain INPP4B
nsv1027781 Chr.4:142022332 - 142385414 on Build GRCh38 Gain INPP4B
nsv830096 Chr.4:141945946 - 142102608 on Build GRCh38 Gain INPP4B

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More Information


Additional Information:

For this assay, SNP(s) [rs201809932] 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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