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

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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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