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          • Home
          • › Search Tool
          • › Search Results
          • › Hs05152018_cn
          See other PAPSS2 CNV Assays ›
          Gene Symbol
          PAPSS2
          Assay Reference Genome
          Location

          Chr.10:87675081 on build GRCh38
          Cytoband
          Assay ID Hs05152018_cn
          Size
          Availability Made To Order
          Catalog # 4400291
          Price
          Your Price
          Online offer:
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          • Genomic Map
          • Assay Details
          • More Information

          Genomic Map

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          Assay Details

          Target Gene Details

          Entrez Gene ID:

          9060

          Gene Name:

          3'-phosphoadenosine 5'-phosphosulfate synthase 2

          Gene Aliases:

          ATPSK2, BCYM4, SK2

          Location:

          Chr.10:87659878-87747705 on Build GRCh38

          Assay Gene Location:

          Within Intron 1
          Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
          PAPSS2 NM_001015880.2 NP_001015880.1
          NM_004670.4 NP_004661.2
          AF074331.1 AAD38423.1
          AF150754.2 AAF20366.2
          AF173365.1 AAF12761.1
          AF313907.1 AAK00296.1
          AK301453.1 BAG62977.1
          AK309262.1
          AK312556.1 BAG35453.1
          BC009894.2 AAH09894.1
          BQ221395.1
          CB960618.1
          GQ891452.1 ADO22314.1

          Target Copy Number Variation Details

          DGV Version:

          Release date: 2025-12-01, GRCh GRCh38
          Target
          Variation
          Location CNV
          Subtype
          Genes
          esv3891880 Chr.10:87343291 - 87725505 on Build GRCh38 Gain MINPP1 MIR4678 LINC00863 PAPSS2 FAM245A NUTM2D
          nsv3116547 Chr.10:87666391 - 87676279 on Build GRCh38 Deletion PAPSS2

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          More Information


          Additional Information:

          For this assay, SNP(s) [rs114585050] 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 Intronic Non-exonic DGV Variation

          Gene Ontology Categories:

          Function(s) Process(es)

          sulfate assimilation
          hormone metabolic process
          3'-phosphoadenosine 5'-phosphosulfate biosynthetic process
          nucleotide binding
          catalytic activity
          adenylylsulfate kinase activity
          sulfate adenylyltransferase (ATP) activity
          protein binding
          ATP binding
          kinase activity
          transferase activity
          nucleotidyltransferase activity

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