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          • Home
          • › Search Tool
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          • › Hs03830862_cn
          See other SLC2A14 CNV Assays ›
          Gene Symbol
          SLC2A14
          Assay Reference Genome
          Location

          Chr.12:7871558 on build GRCh38
          Cytoband
          12p13.31
          Assay ID Hs03830862_cn
          Size
          Availability Made To Order
          Catalog # 4400291
          Price
          Your Price
          Online offer:
          Check your price ›
          • Genomic Map
          • Assay Details
          • More Information

          Genomic Map

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          Assay Details

          Target Gene Details

          Entrez Gene ID:

          144195

          Gene Name:

          solute carrier family 2 member 14

          Gene Aliases:

          GLUT14, SLC2A3P3

          Location:

          Chr.12:7812512-7891196 on Build GRCh38

          Assay Gene Location:

          Within Intron 5
          Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
          SLC2A14 NM_001286233.1 NP_001273162.1
          NM_001286234.1 NP_001273163.1
          NM_001286235.1 NP_001273164.1
          NM_001286236.1 NP_001273165.1
          NM_001286237.1 NP_001273166.1
          NM_153449.3 NP_703150.1
          XM_005253315.3 XP_005253372.1
          XM_005253317.4 XP_005253374.1
          XM_011520562.1 XP_011518864.1
          XM_011520563.2 XP_011518865.1
          XM_011520564.2 XP_011518866.1
          XM_011520565.2 XP_011518867.1
          XM_017018841.1 XP_016874330.1
          XM_017018842.1 XP_016874331.1
          XM_017018843.1 XP_016874332.1
          XM_017018844.1 XP_016874333.1
          XM_017018845.1 XP_016874334.1
          XM_017018846.1 XP_016874335.1
          XM_017018847.1 XP_016874336.1
          AF481878.1 AAL89709.1
          AF481879.1 AAL89710.1
          AK122783.1
          AK126026.1
          AK299037.1
          AK302881.1
          AK316238.1
          AL110298.1 CAB53739.2
          BC060766.1 AAH60766.1
          BG717327.1
          DA723309.1
          DB061127.1
          DB062960.1
          DB069339.1
          DB082816.1

          Target Copy Number Variation Details

          DGV Version:

          Release date: 2016-05-15, GRCh GRCh38
          Target
          Variation
          Location CNV
          Subtype
          Genes
          esv2656717 Chr.12:7798646 - 7905603 on Build GRCh38 Deletion SLC2A14 NANOGP1
          dgv2334n54 Chr.12:7847740 - 7950607 on Build GRCh38 Loss SLC2A14 SLC2A3 NANOGP1
          esv2751114 Chr.12:7810616 - 7964473 on Build GRCh38 Loss SLC2A14 SLC2A3 NANOGP1
          esv3580097 Chr.12:7851816 - 7971452 on Build GRCh38 Loss SLC2A14 SLC2A3 NANOGP1
          nsv826225 Chr.12:7845109 - 7974566 on Build GRCh38 Gain SLC2A14 SLC2A3 NANOGP1
          dgv59e55 Chr.12:7864877 - 7989987 on Build GRCh38 Gain SLC2A14 SLC2A3 NANOGP1
          nsv1035735 Chr.12:7851817 - 7882543 on Build GRCh38 Gain SLC2A14
          esv29743 Chr.12:7842682 - 7970710 on Build GRCh38 Gain SLC2A14 SLC2A3 NANOGP1
          dgv61n111 Chr.12:7811433 - 7978362 on Build GRCh38 Duplication SLC2A14 SLC2A3 NANOGP1
          esv3628446 Chr.12:7850660 - 7872389 on Build GRCh38 Loss SLC2A14
          esv2745493 Chr.12:7778330 - 7906182 on Build GRCh38 Deletion SLC2A14 NANOGP1 NANOG
          dgv6e196 Chr.12:7670828 - 7920436 on Build GRCh38 Duplication DPPA3 NANOGNB SLC2A14 SLC2A3 NANOGP1 GDF3 CLEC4C NANOG
          nsv470265 Chr.12:7840720 - 7970710 on Build GRCh38 Loss SLC2A14 SLC2A3 NANOGP1
          nsv818883 Chr.12:7832345 - 7916285 on Build GRCh38 Gain SLC2A14 NANOGP1
          dgv2335n54 Chr.12:7848316 - 7973149 on Build GRCh38 Loss SLC2A14 SLC2A3 NANOGP1
          esv3548706 Chr.12:7842215 - 7980904 on Build GRCh38 Deletion SLC2A14 SLC2A3 NANOGP1
          esv3628445 Chr.12:7847526 - 8064130 on Build GRCh38 Gain C3AR1 FOXJ2 SLC2A14 SLC2A3 NANOGP1
          dgv58e55 Chr.12:7801455 - 7987805 on Build GRCh38 Gain SLC2A14 SLC2A3 NANOGP1
          dgv2336n54 Chr.12:7869336 - 7938243 on Build GRCh38 Loss SLC2A14 SLC2A3 NANOGP1
          esv2759877 Chr.12:7704223 - 8471391 on Build GRCh38 Gain+Loss DPPA3 POU5F1P3 FAM90A1 FAM86FP LINC00937 FOXJ2 SLC2A14 CLEC6A NANOGP1 C3AR1 FAM66C NANOGNB NECAP1 SLC2A3 LOC101927905 CLEC4C NANOG CLEC4A ZNF705A
          dgv2329n54 Chr.12:7808980 - 7993566 on Build GRCh38 Gain SLC2A14 SLC2A3 NANOGP1
          nsv1070090 Chr.12:7798719 - 7905639 on Build GRCh38 Deletion SLC2A14 NANOGP1
          dgv60e55 Chr.12:7864882 - 7982073 on Build GRCh38 Loss SLC2A14 SLC2A3 NANOGP1
          dgv11e213 Chr.12:7851829 - 7987805 on Build GRCh38 Gain SLC2A14 SLC2A3 NANOGP1
          dgv1354n100 Chr.12:7842179 - 7952475 on Build GRCh38 Gain SLC2A14 SLC2A3 NANOGP1
          dgv166e201 Chr.12:7827227 - 7939801 on Build GRCh38 Deletion SLC2A14 SLC2A3 NANOGP1
          dgv179n27 Chr.12:7818125 - 7946706 on Build GRCh38 Gain SLC2A14 SLC2A3 NANOGP1
          dgv2328n54 Chr.12:7800493 - 7935631 on Build GRCh38 Gain SLC2A14 SLC2A3 NANOGP1
          dgv1351n100 Chr.12:7801358 - 7927734 on Build GRCh38 Gain SLC2A14 SLC2A3 NANOGP1
          esv2760250 Chr.12:7842191 - 7978362 on Build GRCh38 Gain SLC2A14 SLC2A3 NANOGP1
          dgv167e201 Chr.12:7842493 - 7972788 on Build GRCh38 Deletion SLC2A14 SLC2A3 NANOGP1
          esv3580494 Chr.12:7799167 - 7908106 on Build GRCh38 Gain SLC2A14 NANOGP1
          nsv975644 Chr.12:7843169 - 7915838 on Build GRCh38 Duplication SLC2A14 NANOGP1
          dgv449e212 Chr.12:7821394 - 7989987 on Build GRCh38 Gain SLC2A14 SLC2A3 NANOGP1
          dgv1352n100 Chr.12:7805181 - 7978362 on Build GRCh38 Gain SLC2A14 SLC2A3 NANOGP1
          esv3892130 Chr.12:7824755 - 7923089 on Build GRCh38 Gain+Loss SLC2A14 SLC2A3 NANOGP1
          dgv183n27 Chr.12:7844294 - 7973149 on Build GRCh38 Loss SLC2A14 SLC2A3 NANOGP1
          dgv57e55 Chr.12:7700916 - 7963472 on Build GRCh38 Gain DPPA3 NANOGNB SLC2A14 SLC2A3 NANOGP1 CLEC4C NANOG
          dgv5e196 Chr.12:7621924 - 7954221 on Build GRCh38 Duplication DPPA3 NANOGNB SLC2A14 SLC2A3 NANOGP1 GDF3 CLEC4C NANOG APOBEC1

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          More Information


          Set Membership:

          Intragenic Intronic Non-exonic DGV Variation

          Gene Ontology Categories:

          Function(s) Process(es)

          multicellular organism development
          spermatogenesis
          cell differentiation
          glucose transmembrane transport
          glucose transmembrane transporter activity

          Back To Top

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