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See other FKBP9 CNV Assays ›
Gene Symbol
FKBP9
Assay Reference Genome
Location

Chr.7:32957503 on build GRCh38
Cytoband
7p14.3
Assay ID Hs04342281_cn
Size
Availability Made To Order
Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 11328

Gene Name:

 FK506 binding protein 9

Gene Aliases:

 FKBP60, FKBP63, PPIase

Location:

 Chr.7:32957404-33006931 on Build GRCh38

Assay Gene Location:

 Within Exon 1
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
FKBP9 NM_001284341.1 1 100 NP_001271270.1
NM_007270.4 1 100 NP_009201.2
XM_011515115.2 1 100 XP_011513417.1
AK075331.1 1 64
AK128597.1
AK293954.1 1 30
AK294266.1 1 30
AK300328.1 1 63
BC101723.1 1 28 AAI01724.1
BC112053.1 1 28 AAI12054.1
DA234297.1 1 100
DC317549.1 1 137

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv1029220 Chr.7:32881872 - 33222578 on Build GRCh38 Gain FKBP9 RP9 NT5C3A BBS9 KBTBD2 RP9P
dgv1080e201 Chr.7:32621750 - 35008557 on Build GRCh38 Deletion DPY19L1P1 ZNRF2P1 DPY19L1 DPY19L1P2 FLJ20712 NT5C3A MIR550B2 BBS9 MIR548N BMPER RP9P NPSR1-AS1 LOC100421336 FKBP9 RP9 LINC00997 NPSR1 MIR550A2 KBTBD2
esv2734229 Chr.7:32916268 - 33093711 on Build GRCh38 Deletion FKBP9 NT5C3A RP9P
nsv1135982 Chr.7:32794601 - 34893593 on Build GRCh38 Deletion LOC100421336 FKBP9 DPY19L1P2 FLJ20712 RP9 NPSR1 NT5C3A BBS9 BMPER KBTBD2 RP9P NPSR1-AS1
nsv1033096 Chr.7:32925428 - 32999594 on Build GRCh38 Loss FKBP9 RP9P
nsv436907 Chr.7:32668474 - 34999437 on Build GRCh38 Insertion DPY19L1P1 ZNRF2P1 DPY19L1 DPY19L1P2 FLJ20712 NT5C3A MIR550B2 BBS9 MIR548N BMPER RP9P NPSR1-AS1 LOC100421336 FKBP9 RP9 LINC00997 NPSR1 MIR550A2 KBTBD2

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More Information


Additional Information:

For this assay, SNP(s) [rs527879179] 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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