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          • Home
          • › Search Tool
          • › Search Results
          • › Hs03417107_cn
          See other ACP1 CNV Assays ›
          Gene Symbol
          ACP1
          Assay Reference Genome
          Location

          Chr.2:276640 on build GRCh38
          Cytoband
          2p25.3
          Assay ID Hs03417107_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:

          52

          Gene Name:

          acid phosphatase 1, soluble

          Gene Aliases:

          HAAP, LMW-PTP

          Location:

          Chr.2:264869-278283 on Build GRCh38

          Assay Gene Location:

          Within Intron 4
          Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
          ACP1 NM_004300.3 NP_004291.1
          NM_007099.3 NP_009030.1
          NR_024080.1
          AB209838.1 BAD93075.1
          AK289934.1
          AK291861.1
          BC007422.2 AAH07422.1
          BC106011.1 AAI06012.1
          BI460080.1
          BJ992018.1
          BT007136.1 AAP35800.1
          DB443811.1
          M83653.1 AAB59354.1
          M83654.1 AAB59355.1
          M87545.1
          S62884.1 AAB27085.1
          Y16846.1 CAA76416.1

          Target Copy Number Variation Details

          DGV Version:

          Release date: 2016-05-15, GRCh GRCh38
          Target
          Variation
          Location CNV
          Subtype
          Genes
          esv3589599 Chr.2:251988 - 283726 on Build GRCh38 Gain SH3YL1 FAM150B ACP1
          esv3589598 Chr.2:250064 - 298533 on Build GRCh38 Gain SH3YL1 FAM150B ACP1 LOC101927262
          dgv3698n100 Chr.2:265970 - 313392 on Build GRCh38 Gain FAM150B ACP1 LOC101927262
          nsv833159 Chr.2:158491 - 327294 on Build GRCh38 Loss SH3YL1 FAM150B ACP1 LOC101927262
          nsv833170 Chr.2:274456 - 471195 on Build GRCh38 Loss FAM150B ACP1 LOC101927262
          esv2759016 Chr.2:167949 - 929902 on Build GRCh38 Gain LOC101060385 SH3YL1 TMEM18 FAM150B LOC105373392 LOC105373480 LOC105373352 LOC101927362 ACP1 LOC101927262 LOC100996637 LINC01115

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          More Information


          Set Membership:

          Intragenic Intronic Non-exonic DGV Variation

          Panther Classification:

          Molecular Function -

          protein phosphatase protein modifying enzyme

          Gene Ontology Categories:

          Function(s) Process(es)

          peptidyl-tyrosine dephosphorylation
          acid phosphatase activity
          non-membrane spanning protein tyrosine phosphatase activity
          protein binding

          Back To Top

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