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          • › Hs01926279_cn
          See other STARD7 CNV Assays ›
          Gene Symbol
          STARD7
          Assay Reference Genome
          Location

          Chr.2:96185506 on build GRCh38
          Cytoband
          Assay ID Hs01926279_cn
          Size
          Availability Made To Order
          Catalog # 4400291
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          • Genomic Map
          • Assay Details
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          Genomic Map

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          Assay Details

          Target Gene Details

          Entrez Gene ID:

          56910

          Gene Name:

          StAR related lipid transfer domain containing 7

          Gene Aliases:

          ADCME, BAFME2, FAME, FAME2, FCMTE2, GTT1

          Location:

          Chr.2:96184859-96208827 on Build GRCh38

          Assay Gene Location:

          Within Exon 8
          Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
          STARD7 NM_001385622.1 8 2336 NP_001372551.1
          NM_020151.4 8 2730 NP_064536.2
          AB075479.1 1 364
          AF270647.1 8 2665 AAF81750.1
          AK023234.1 7 1997
          AK054615.1 8 2104 BAG51400.1
          AK094925.1 2 2310
          AK096666.1 5 1498
          BC007894.2 9 2496 AAH07894.1
          BC008894.2 8 2721 AAH08894.1
          BC009998.2 9 2496 AAH09998.1
          BC012774.2 8 2688 AAH12774.1
          BC012793.2 8 2702 AAH12793.1
          BC013279.2 8 2721 AAH13279.1
          BC014076.2 8 2698 AAH14076.1
          BC014274.2 8 2717 AAH14274.3
          BC032106.1 8 2712 AAH32106.1
          CR749695.1 1 1053

          Target Copy Number Variation Details

          DGV Version:

          Release date: 2025-12-01, GRCh GRCh38
          Target
          Variation
          Location CNV
          Subtype
          Genes
          nsv4738830 Chr.2:96068807 - 97624627 on Build GRCh38 Deletion LOC105373496 STARD7 LOC124908044 FAM178B KANSL3 ARID5A NCAPH FAHD2B LMAN2L LOC101927053 APPAT NEURL3 MIR3127 CNNM4 ITPRIPL1 ANKRD36 ANKRD36B SEMA4C ANKRD39 ANKRD23 STARD7-AS1 ADRA2B SNORA112 GPAT2P2 FER1L5 LOC100506076 CNNM3-DT DUSP2 SNRNP200 TMEM127 CIAO1 ASTL CNNM3
          nsv834305 Chr.2:96183160 - 96353738 on Build GRCh38 Gain STARD7 SNRNP200 STARD7-AS1 ITPRIPL1 TMEM127 CIAO1 NCAPH SNORA112
          nsv4057575 Chr.2:96060952 - 97147263 on Build GRCh38 Duplication LOC105373496 STARD7 LOC124908044 FAM178B KANSL3 ARID5A NCAPH FAHD2B LMAN2L LOC101927053 NEURL3 MIR3127 CNNM4 ITPRIPL1 ANKRD36 SEMA4C ANKRD39 ANKRD23 STARD7-AS1 ADRA2B SNORA112 GPAT2P2 FER1L5 CNNM3-DT DUSP2 SNRNP200 TMEM127 CIAO1 ASTL CNNM3
          dgv607e201 Chr.2:95855884 - 97561622 on Build GRCh38 Deletion LOC105373496 STARD7 LOC124908044 FAM178B KANSL3 ARID5A NCAPH FAHD2B LMAN2L LOC101927053 APPAT LOC124900512 ANKRD36C NEURL3 MIR3127 CNNM4 ITPRIPL1 GPAT2 ANKRD36 ANKRD36B SEMA4C ANKRD39 ANKRD23 STARD7-AS1 ADRA2B SNORA112 GPAT2P2 FER1L5 LOC100506076 CNNM3-DT DUSP2 SNRNP200 TMEM127 CIAO1 ASTL CNNM3 FAHD2CP
          nsv5876678 Chr.2:95981467 - 97579646 on Build GRCh38 Deletion LOC105373496 STARD7 LOC124908044 FAM178B KANSL3 ARID5A NCAPH FAHD2B LMAN2L LOC101927053 APPAT LOC124900512 ANKRD36C NEURL3 MIR3127 CNNM4 ITPRIPL1 GPAT2 ANKRD36 ANKRD36B SEMA4C ANKRD39 ANKRD23 STARD7-AS1 ADRA2B SNORA112 GPAT2P2 FER1L5 LOC100506076 CNNM3-DT DUSP2 SNRNP200 TMEM127 CIAO1 ASTL CNNM3 FAHD2CP
          nsv1135873 Chr.2:95981454 - 97579645 on Build GRCh38 Deletion LOC105373496 STARD7 LOC124908044 FAM178B KANSL3 ARID5A NCAPH FAHD2B LMAN2L LOC101927053 APPAT LOC124900512 ANKRD36C NEURL3 MIR3127 CNNM4 ITPRIPL1 GPAT2 ANKRD36 ANKRD36B SEMA4C ANKRD39 ANKRD23 STARD7-AS1 ADRA2B SNORA112 GPAT2P2 FER1L5 LOC100506076 CNNM3-DT DUSP2 SNRNP200 TMEM127 CIAO1 ASTL CNNM3 FAHD2CP
          esv3425717 Chr.2:95859900 - 97515905 on Build GRCh38 Duplication LOC105373496 STARD7 LOC124908044 FAM178B KANSL3 ARID5A NCAPH FAHD2B LMAN2L LOC101927053 APPAT LOC124900512 ANKRD36C NEURL3 MIR3127 CNNM4 ITPRIPL1 GPAT2 ANKRD36 ANKRD36B SEMA4C ANKRD39 ANKRD23 STARD7-AS1 ADRA2B SNORA112 GPAT2P2 FER1L5 LOC100506076 CNNM3-DT DUSP2 SNRNP200 TMEM127 CIAO1 ASTL CNNM3 FAHD2CP

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          More Information


          Set Membership:

          Intragenic Exonic DGV Variation

          Gene Ontology Categories:

          Function(s) Process(es)

          myeloid dendritic cell activation
          ubiquinone biosynthetic process
          inflammatory response
          type 2 immune response
          establishment of skin barrier
          intermembrane lipid transfer
          mucociliary clearance
          protein binding
          lipid binding
          intermembrane lipid transfer activity
          molecular carrier activity

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