Assay Details
Target Gene Details
Entrez Gene ID: | 339501 |
Gene Name: | protease, serine 38 |
Gene Aliases: |
MPN2 |
Location: |
Chr.1:227815708-227846470 on Build GRCh38 |
Assay Gene Location: | Within Exon 3 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
PRSS38 | NM_183062.2 | 3 | 496 | NP_898885.1 |
XM_011544175.2 | 3 | 505 | XP_011542477.1 | |
XM_011544176.2 | 3 | 505 | XP_011542478.1 | |
BC130400.1 | 3 | 568 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv549273 | Chr.1:227808265 - 227863533 on Build GRCh38 | Loss |
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nsv826908 | Chr.1:227707685 - 228503399 on Build GRCh38 | Gain |
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esv32853 | Chr.1:227692415 - 228670462 on Build GRCh38 | Gain |
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nsv998933 | Chr.1:227805227 - 227871595 on Build GRCh38 | Loss |
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nsv549272 | Chr.1:227748061 - 227858047 on Build GRCh38 | Loss |
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![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)
More Information
Additional Information:
For this assay, SNP(s) [rs74588116] 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: |
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Panther Classification:
Gene Ontology Categories:
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