Assay Details
Target Gene Details
Entrez Gene ID: | 56910 |
Gene Name: | StAR related lipid transfer domain containing 7 |
Gene Aliases: |
GTT1 |
Location: |
Chr.2:96184859-96208846 on Build GRCh38 |
Assay Gene Location: | Within Exon 8 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
STARD7 | NM_020151.3 | 8 | 2266 | NP_064536.2 |
XM_011511499.1 | 8 | 1883 | XP_011509801.1 | |
AF270647.1 | 8 | 2193 | AAF81750.1 | |
AK023234.1 | 7 | 1525 | ||
AK054615.1 | 8 | 1632 | ||
AK094925.1 | 2 | 1838 | ||
AK096666.1 | 5 | 1026 | ||
BC007894.2 | 9 | 2024 | AAH07894.1 | |
BC008894.2 | 8 | 2249 | AAH08894.1 | |
BC009998.2 | 9 | 2024 | AAH09998.1 | |
BC012774.2 | 8 | 2216 | AAH12774.1 | |
BC012793.2 | 8 | 2230 | AAH12793.1 | |
BC013279.2 | 8 | 2249 | AAH13279.1 | |
BC014076.2 | 8 | 2226 | AAH14076.1 | |
BC014274.2 | 8 | 2245 | AAH14274.3 | |
BC032106.1 | 8 | 2240 | AAH32106.1 | |
CR749695.1 | 1 | 581 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv834305 | Chr.2:96183160 - 96353738 on Build GRCh38 | Gain | TMEM127 NCAPH ITPRIPL1 LOC105373495 SNRNP200 STARD7 STARD7-AS1 CIAO1 |
dgv607e201 | Chr.2:95855884 - 97561622 on Build GRCh38 | Deletion | TMEM127 FAM178B STARD7 LMAN2L FAHD2CP DUSP2 ANKRD39 LOC100506076 ANKRD36C NCAPH LOC105373495 ANKRD36 CNNM4 LOC100506123 NEURL3 ANKRD36B KANSL3 FER1L5 ARID5A LOC653924 ADRA2B ANKRD23 LOC107984110 ASTL GPAT2 SEMA4C FAHD2B CIAO1 ITPRIPL1 SNRNP200 LOC101927053 STARD7-AS1 CNNM3 LOC105373496 MIR3127 |
nsv1135873 | Chr.2:95981454 - 97579645 on Build GRCh38 | Deletion | TMEM127 FAM178B STARD7 LMAN2L FAHD2CP DUSP2 ANKRD39 LOC100506076 ANKRD36C NCAPH LOC105373495 ANKRD36 CNNM4 LOC100506123 NEURL3 ANKRD36B KANSL3 FER1L5 ARID5A LOC653924 ADRA2B ANKRD23 LOC107984110 ASTL GPAT2 SEMA4C FAHD2B CIAO1 ITPRIPL1 SNRNP200 LOC101927053 STARD7-AS1 CNNM3 LOC105373496 MIR3127 |
esv3425717 | Chr.2:95859900 - 97515905 on Build GRCh38 | Duplication | TMEM127 FAM178B STARD7 LMAN2L FAHD2CP DUSP2 ANKRD39 LOC100506076 ANKRD36C NCAPH LOC105373495 ANKRD36 CNNM4 LOC100506123 NEURL3 ANKRD36B KANSL3 FER1L5 ARID5A LOC653924 ADRA2B ANKRD23 LOC107984110 ASTL GPAT2 SEMA4C FAHD2B CIAO1 ITPRIPL1 SNRNP200 LOC101927053 STARD7-AS1 CNNM3 LOC105373496 MIR3127 |
More Information
Set Membership: |
Intragenic Exonic DGV Variation |