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          • › Search Tool
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          • › Hs01815251_cn
          See other STARD7 CNV Assays ›
          Gene Symbol
          STARD7
          Assay Reference Genome
          Location

          Chr.2:96208307 on build GRCh38
          Cytoband
          Assay ID Hs01815251_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 Exon 1
          Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
          STARD7 NM_001385622.1 NP_001372551.1
          NM_020151.4 1 521 NP_064536.2
          AF270647.1 1 464 AAF81750.1
          AL542720.3 1 535
          BC007894.2 2 287 AAH07894.1
          BC008894.2 1 512 AAH08894.1
          BC009998.2 2 287 AAH09998.1
          BC012774.2 1 479 AAH12774.1
          BC012793.2 1 493 AAH12793.1
          BC013279.2 1 512 AAH13279.1
          BC014076.2 1 489 AAH14076.1
          BC014274.2 1 508 AAH14274.3
          BC032106.1 1 503 AAH32106.1
          CN394859.1 1 529

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

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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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