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See other PRSS57 CNV Assays ›
Gene Symbol
PRSS57
Assay Reference Genome
Location

Chr.19:687037 on build GRCh38
Cytoband
19p13.3
Assay ID Hs01423428_cn
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Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 400668

Gene Name:

 protease, serine 57

Gene Aliases:

 NSP4, PRSSL1, UNQ782

Location:

 Chr.19:685521-695461 on Build GRCh38

Assay Gene Location:

 Within Exon 4
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
PRSS57 NM_001308209.1 4 561 NP_001295138.1
NM_214710.4 4 564 NP_999875.1
AY358594.1 4 601 AAQ88957.1
BC137161.1 4 566
BC144505.1 4 563

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv428360 Chr.19:232069 - 702131 on Build GRCh38 Gain FGF22 THEG FSTL3 ODF3L2 HCN2 GZMM PRSS57 LOC101929060 CDC34 POLRMT MIER2 BSG SHC2 PLPP2 TPGS1 RNF126 MADCAM1 C2CD4C
dgv134n111 Chr.19:607984 - 967584 on Build GRCh38 Deletion FGF22 MIR4745 FSTL3 HCN2 PRTN3 KISS1R R3HDM4 PRSS57 MISP PTBP1 ARID3A PALM ELANE LOC101928450 PLPPR3 AZU1 POLRMT CFD MIR3187 RNU6-9 MED16 RNF126
nsv577978 Chr.19:294526 - 782854 on Build GRCh38 Gain FGF22 THEG FSTL3 ODF3L2 HCN2 GZMM PRSS57 MISP LOC101929060 CDC34 PALM LOC101928450 POLRMT MIER2 BSG SHC2 TPGS1 RNF126 MADCAM1 C2CD4C
nsv953938 Chr.19:355801 - 1104501 on Build GRCh38 Deletion FGF22 THEG ODF3L2 GRIN3B PRTN3 KISS1R GZMM PRSS57 ABCA7 ARHGAP45 PTBP1 ARID3A LOC105372235 CDC34 PALM ELANE LOC101928450 AZU1 BSG RNU6-9 SHC2 MED16 WDR18 MADCAM1 MIR4745 FSTL3 HCN2 R3HDM4 RNU6-2 POLR2E MISP TMEM259 CNN2 PLPPR3 POLRMT CFD MIR3187 GPX4 TPGS1 RNF126 C2CD4C
nsv470101 Chr.19:401714 - 1008505 on Build GRCh38 Loss FGF22 ODF3L2 GRIN3B PRTN3 KISS1R GZMM PRSS57 PTBP1 ARID3A LOC105372235 CDC34 PALM ELANE LOC101928450 AZU1 BSG RNU6-9 SHC2 MED16 WDR18 MADCAM1 MIR4745 FSTL3 HCN2 R3HDM4 MISP PLPPR3 POLRMT CFD MIR3187 TPGS1 RNF126 C2CD4C

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More Information


Additional Information:

For this assay, SNP(s) [rs72618587] 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:

Gene Ontology Categories:

Function(s) Process(es)


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