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See other SERPINA9 CNV Assays ›
Gene Symbol
SERPINA9
Assay Reference Genome
Location

Chr.14:94469289 on build GRCh38
Cytoband
14q32.13
Assay ID Hs01830137_cn
Size
Availability Made To Order
Catalog # 4400291
Price
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Assay Details

Target Gene Details

Entrez Gene ID:

 327657

Gene Name:

 serpin family A member 9

Gene Aliases:

 GCET1, SERPINA11, SERPINA11b

Location:

 Chr.14:94462721-94476333 on Build GRCh38

Assay Gene Location:

 Within Exon 3
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
SERPINA9 NM_001042518.1 NP_001035983.1
NM_001284275.1 2 577 NP_001271204.1
NM_001284276.1 3 474 NP_001271205.1
NM_175739.3 2 767 NP_783866.2
XM_011536714.2 2 873 XP_011535016.1
XM_011536715.2 3 737 XP_011535017.1
XM_011536716.2 2 683 XP_011535018.1
XM_011536717.1 2 1566 XP_011535019.1
AK301082.1 2 661
AY185496.1 2 767 AAO32345.1
AY185497.1 2 577 AAO32346.1
AY220118.1 2 681 AAO65242.1
AY220119.1 AAO65243.1
AY220120.1 2 442 AAO65244.1
AY220121.1 3 383 AAO65245.1
AY358700.1 2 611 AAQ89063.1
BC111498.1 2 670 AAI11499.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv832863 Chr.14:94348482 - 94501487 on Build GRCh38 Gain SERPINA1 SERPINA2 SERPINA9 SERPINA11 SERPINA12
nsv510649 Chr.14:94421103 - 94544514 on Build GRCh38 Deletion SERPINA9 SERPINA11 SERPINA12
nsv470662 Chr.14:94296542 - 94798793 on Build GRCh38 Gain SERPINA13P SERPINA1 SERPINA6 SERPINA2 SERPINA9 SERPINA11 GSC SERPINA12 SERPINA5 SERPINA4 SERPINA3
nsv1407 Chr.14:94450081 - 94477913 on Build GRCh38 Insertion SERPINA9 SERPINA11
nsv565623 Chr.14:94393116 - 94635006 on Build GRCh38 Gain SERPINA9 SERPINA11 SERPINA12 SERPINA5 SERPINA4 SERPINA3
nsv832864 Chr.14:94362101 - 94538150 on Build GRCh38 Loss SERPINA1 SERPINA2 SERPINA9 SERPINA11 SERPINA12

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More Information


Additional Information:

For this assay, SNP(s) [rs78283108] 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

Panther Classification:

Molecular Function -

protease inhibitor

Gene Ontology Categories:

Function(s) Process(es)


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