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          • Home
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          • › Hs03404627_cn
          See other STARD7 CNV Assays ›
          Gene Symbol
          STARD7
          Assay Reference Genome
          Location

          Chr.2:96192039 on build GRCh38
          Cytoband
          Assay ID Hs03404627_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:

          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 Intron 6
          Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
          STARD7 NM_001385622.1 NP_001372551.1
          NM_020151.4 NP_064536.2
          AF270647.1 AAF81750.1
          AK023234.1
          AK054615.1 BAG51400.1
          AK096666.1
          AK291190.1 BAF83879.1
          BC007894.2 AAH07894.1
          BC008894.2 AAH08894.1
          BC009998.2 AAH09998.1
          BC012774.2 AAH12774.1
          BC012793.2 AAH12793.1
          BC013279.2 AAH13279.1
          BC014076.2 AAH14076.1
          BC014274.2 AAH14274.3
          BC032106.1 AAH32106.1

          Target Copy Number Variation Details

          DGV Version:

          Release date: 2025-12-01, GRCh GRCh38
          Target
          Variation
          Location CNV
          Subtype
          Genes
          nsv4060312 Chr.2:96190262 - 96215262 on Build GRCh38 Deletion STARD7 SNORA112 STARD7-AS1
          nsv4738830 Chr.2:96068807 - 97624627 on Build GRCh38 Deletion TMEM127 FER1L5 LOC105373496 SNORA112 ITPRIPL1 CNNM3 MIR3127 NCAPH ANKRD23 ANKRD39 KANSL3 GPAT2P2 LOC124908044 STARD7 NEURL3 FAM178B ADRA2B DUSP2 FAHD2B LOC101927053 ASTL CNNM4 ARID5A LMAN2L SEMA4C ANKRD36B LOC100506076 CIAO1 CNNM3-DT ANKRD36 APPAT SNRNP200 STARD7-AS1
          nsv834305 Chr.2:96183160 - 96353738 on Build GRCh38 Gain STARD7 NCAPH TMEM127 CIAO1 SNORA112 ITPRIPL1 SNRNP200 STARD7-AS1
          nsv4057575 Chr.2:96060952 - 97147263 on Build GRCh38 Duplication TMEM127 FER1L5 LOC105373496 SNORA112 ITPRIPL1 CNNM3 MIR3127 NCAPH ANKRD23 ANKRD39 KANSL3 GPAT2P2 LOC124908044 STARD7 NEURL3 FAM178B ADRA2B DUSP2 FAHD2B LOC101927053 ASTL CNNM4 ARID5A LMAN2L SEMA4C CIAO1 CNNM3-DT ANKRD36 SNRNP200 STARD7-AS1
          dgv607e201 Chr.2:95855884 - 97561622 on Build GRCh38 Deletion FAHD2CP TMEM127 FER1L5 LOC105373496 SNORA112 ITPRIPL1 CNNM3 MIR3127 NCAPH ANKRD23 ANKRD39 ANKRD36C KANSL3 GPAT2P2 LOC124908044 STARD7 NEURL3 FAM178B ADRA2B DUSP2 FAHD2B LOC101927053 ASTL CNNM4 ARID5A LMAN2L SEMA4C ANKRD36B LOC100506076 CIAO1 GPAT2 CNNM3-DT ANKRD36 APPAT SNRNP200 LOC124900512 STARD7-AS1
          nsv5876678 Chr.2:95981467 - 97579646 on Build GRCh38 Deletion FAHD2CP TMEM127 FER1L5 LOC105373496 SNORA112 ITPRIPL1 CNNM3 MIR3127 NCAPH ANKRD23 ANKRD39 ANKRD36C KANSL3 GPAT2P2 LOC124908044 STARD7 NEURL3 FAM178B ADRA2B DUSP2 FAHD2B LOC101927053 ASTL CNNM4 ARID5A LMAN2L SEMA4C ANKRD36B LOC100506076 CIAO1 GPAT2 CNNM3-DT ANKRD36 APPAT SNRNP200 LOC124900512 STARD7-AS1
          nsv1135873 Chr.2:95981454 - 97579645 on Build GRCh38 Deletion FAHD2CP TMEM127 FER1L5 LOC105373496 SNORA112 ITPRIPL1 CNNM3 MIR3127 NCAPH ANKRD23 ANKRD39 ANKRD36C KANSL3 GPAT2P2 LOC124908044 STARD7 NEURL3 FAM178B ADRA2B DUSP2 FAHD2B LOC101927053 ASTL CNNM4 ARID5A LMAN2L SEMA4C ANKRD36B LOC100506076 CIAO1 GPAT2 CNNM3-DT ANKRD36 APPAT SNRNP200 LOC124900512 STARD7-AS1
          esv3425717 Chr.2:95859900 - 97515905 on Build GRCh38 Duplication FAHD2CP TMEM127 FER1L5 LOC105373496 SNORA112 ITPRIPL1 CNNM3 MIR3127 NCAPH ANKRD23 ANKRD39 ANKRD36C KANSL3 GPAT2P2 LOC124908044 STARD7 NEURL3 FAM178B ADRA2B DUSP2 FAHD2B LOC101927053 ASTL CNNM4 ARID5A LMAN2L SEMA4C ANKRD36B LOC100506076 CIAO1 GPAT2 CNNM3-DT ANKRD36 APPAT SNRNP200 LOC124900512 STARD7-AS1

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          More Information


          Set Membership:

          Intragenic Intronic Non-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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