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          • Home
          • › Search Tool
          • › Search Results
          • › Hs06666104_cn
          See other SUMF1 CNV Assays ›
          Gene Symbol
          SUMF1
          Assay Reference Genome
          Location

          Chr.3:4034852 on build GRCh38
          Cytoband
          Assay ID Hs06666104_cn
          Size
          Availability Made To Order
          Catalog # 4400291
          Price
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          • Genomic Map
          • Assay Details
          • More Information

          Genomic Map

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          Assay Details

          Target Gene Details

          Entrez Gene ID:

          285362

          Gene Name:

          sulfatase modifying factor 1

          Gene Aliases:

          AAPA3037, FGE, UNQ3037

          Location:

          Chr.3:4034486-4467269 on Build GRCh38

          Assay Gene Location:

          Within Intron 14
          Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
          SUMF1 XM_017006254.3 XP_016861743.1
          AY358092.1 AAQ88459.1

          Target Copy Number Variation Details

          DGV Version:

          Release date: 2025-12-01, GRCh GRCh38
          Target
          Variation
          Location CNV
          Subtype
          Genes
          nsv4077045 Chr.3:3819660 - 4285363 on Build GRCh38 Duplication SUMF1 LRRN1
          dgv4762n223 Chr.3:3857761 - 4141396 on Build GRCh38 Deletion SUMF1
          esv2763711 Chr.3:3921859 - 4227347 on Build GRCh38 Loss SUMF1
          dgv4643n100 Chr.3:4034252 - 4087317 on Build GRCh38 Loss SUMF1
          dgv588n27 Chr.3:4019253 - 4218633 on Build GRCh38 Loss SUMF1
          nsv6370818 Chr.3:4034183 - 4036815 on Build GRCh38 Deletion SUMF1
          dgv1438n209 Chr.3:4002099 - 4219002 on Build GRCh38 Deletion SUMF1
          esv3893633 Chr.3:3989971 - 4036970 on Build GRCh38 Gain+Loss SUMF1
          nsv3209225 Chr.3:4011410 - 4043211 on Build GRCh38 Deletion SUMF1
          dgv4766n223 Chr.3:4009545 - 4114078 on Build GRCh38 Deletion SUMF1
          nsv460337 Chr.3:4032349 - 4124049 on Build GRCh38 Loss SUMF1
          dgv1439n209 Chr.3:4030576 - 4133717 on Build GRCh38 Deletion SUMF1
          nsv528048 Chr.3:3957986 - 4171349 on Build GRCh38 Loss SUMF1
          dgv4638n100 Chr.3:3858107 - 4099559 on Build GRCh38 Loss SUMF1
          dgv4641n100 Chr.3:3934721 - 4221511 on Build GRCh38 Loss SUMF1
          dgv1591n166 Chr.3:3962495 - 4192313 on Build GRCh38 Deletion SUMF1
          nsv1005259 Chr.3:3992384 - 4073417 on Build GRCh38 Loss SUMF1
          nsv6356389 Chr.3:4023139 - 4052579 on Build GRCh38 Deletion SUMF1
          dgv8176n54 Chr.3:4034049 - 4062242 on Build GRCh38 Loss SUMF1
          nsv5449395 Chr.3:4030578 - 4163790 on Build GRCh38 Deletion SUMF1
          nsv4083558 Chr.3:4023866 - 4313333 on Build GRCh38 Deletion SETMAR SUMF1
          nsv508208 Chr.3:4012241 - 4069026 on Build GRCh38 Deletion SUMF1
          nsv589407 Chr.3:4000518 - 4107492 on Build GRCh38 Loss SUMF1
          nsv4074346 Chr.3:4021974 - 4040315 on Build GRCh38 Deletion SUMF1
          nsv6368518 Chr.3:4034003 - 4044459 on Build GRCh38 Deletion SUMF1
          dgv4642n100 Chr.3:4019632 - 4112924 on Build GRCh38 Loss SUMF1
          esv3568577 Chr.3:4031410 - 4073001 on Build GRCh38 Loss SUMF1
          esv3893635 Chr.3:3899706 - 4211535 on Build GRCh38 Loss SUMF1
          dgv1592n166 Chr.3:3981800 - 4122959 on Build GRCh38 Deletion SUMF1
          esv3568575 Chr.3:3935472 - 4195417 on Build GRCh38 Loss SUMF1
          dgv4765n223 Chr.3:4006276 - 4217513 on Build GRCh38 Deletion SUMF1
          esv2760789 Chr.3:4024902 - 4194031 on Build GRCh38 Loss SUMF1
          dgv336n206 Chr.3:3883097 - 4082304 on Build GRCh38 Deletion SUMF1
          esv3595075 Chr.3:3957444 - 4160335 on Build GRCh38 Loss SUMF1
          dgv1593n166 Chr.3:4028884 - 4133718 on Build GRCh38 Deletion SUMF1
          dgv4764n223 Chr.3:3933489 - 4219482 on Build GRCh38 Deletion SUMF1
          esv3893636 Chr.3:3985921 - 4094550 on Build GRCh38 Loss SUMF1
          esv3595072 Chr.3:3907300 - 4080268 on Build GRCh38 Loss SUMF1
          nsv5435439 Chr.3:3957458 - 4160267 on Build GRCh38 Deletion SUMF1
          dgv8173n54 Chr.3:3924671 - 4188112 on Build GRCh38 Loss SUMF1
          nsv4082337 Chr.3:4033825 - 4084238 on Build GRCh38 Deletion SUMF1
          nsv3169507 Chr.3:3859793 - 4143342 on Build GRCh38 Deletion SUMF1
          nsv4079044 Chr.3:3859642 - 4039782 on Build GRCh38 Deletion SUMF1
          esv2752004 Chr.3:3979832 - 4163939 on Build GRCh38 Loss SUMF1
          nsv6361210 Chr.3:3988052 - 4076397 on Build GRCh38 Deletion SUMF1
          dgv1590n166 Chr.3:3929380 - 4240992 on Build GRCh38 Deletion SUMF1
          esv3595076 Chr.3:3958327 - 4035443 on Build GRCh38 Loss SUMF1
          nsv589410 Chr.3:4021961 - 4163939 on Build GRCh38 Loss SUMF1

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          More Information


          Set Membership:

          Intragenic Intronic Non-exonic DGV Variation

          Gene Ontology Categories:

          Function(s) Process(es)

          protein oxidation
          post-translational protein modification
          glycosphingolipid catabolic process
          protein binding
          oxidoreductase activity
          identical protein binding
          metal ion binding
          Formylglycine-generating oxidase activity
          cupric ion binding

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